A Novel Class of Tests for the Detection of Mitochondrial DNA–Mutation Involvement in Diseases (Q33904880)

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scientific article published on April 30, 2003

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English	A Novel Class of Tests for the Detection of Mitochondrial DNA–Mutation Involvement in Diseases	scientific article published on April 30, 2003

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instance of

scholarly article

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stated in

Europe PubMed Central

PubMed publication ID

12730827

retrieved

29 July 2017

title

A novel class of tests for the detection of mitochondrial DNA-mutation involvement in diseases (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12730827

retrieved

29 July 2017

A Novel Class of Tests for the Detection of Mitochondrial DNA–Mutation Involvement in Diseases (English)

1 reference

stated in

Crossref

DOI

10.1086/375656

reference URL

https://api.crossref.org/works/10.1086/375656

retrieved

30 December 2023

main subject

mitochondrial DNA

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genetics

1 reference

stated in

Crossref

DOI

10.1086/375656

reference URL

https://api.crossref.org/works/10.1086/375656

retrieved

30 December 2023

author name string

Fengzhu Sun

series ordinal

1

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stated in

Europe PubMed Central

PubMed publication ID

12730827

retrieved

29 July 2017

Jing Cui

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12730827

retrieved

29 July 2017

Haralambos Gavras

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12730827

retrieved

29 July 2017

Faina Schwartz

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12730827

retrieved

29 July 2017

language of work or name

English

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publication date

30 April 2003

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stated in

Europe PubMed Central

PubMed publication ID

12730827

retrieved

29 July 2017

full work available at URL

http://www.cell.com/article/S0002929707604509/pdf

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Portable Document Format

online access status

open access

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12730827

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A12730827

retrieved

30 December 2023

https://europepmc.org/articles/PMC1180311

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HTML

online access status

open access

content deliverer

Europe PubMed Central

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12730827

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A12730827

retrieved

30 December 2023

https://europepmc.org/articles/PMC1180311?pdf=render

file format

Portable Document Format

online access status

open access

content deliverer

Europe PubMed Central

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12730827

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A12730827

retrieved

30 December 2023

https://api.elsevier.com/content/article/PII:S0002929707604509?httpAccept=text/xml

1 reference

stated in

Crossref

DOI

10.1086/375656

reference URL

https://api.crossref.org/works/10.1086/375656

retrieved

30 December 2023

https://api.elsevier.com/content/article/PII:S0002929707604509?httpAccept=text/plain

1 reference

stated in

Crossref

DOI

10.1086/375656

reference URL

https://api.crossref.org/works/10.1086/375656

retrieved

30 December 2023

published in

American Journal of Human Genetics

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12730827

retrieved

29 July 2017

volume

72

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12730827

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29 July 2017

issue

6

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stated in

Europe PubMed Central

PubMed publication ID

12730827

retrieved

29 July 2017

page(s)

1515-1526

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stated in

Europe PubMed Central

PubMed publication ID

12730827

retrieved

29 July 2017

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PubMed Central

reference URL

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The neuropathology of hereditary optic atrophy (Leber's disease); the first complete anatomic study.

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Mutations in mitochondrial cytochrome c oxidase genes segregate with late-onset Alzheimer disease

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Pedigree models for complex human traits involving the mitochondrial genome

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Patterns of maternal transmission in bipolar affective disorder

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Further clinical and pathological observations on Leber's optic atrophy

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28 July 2018

A new manifestation of Leber's disease and a new explanation for the agency responsible for its unusual pattern of inheritance

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Testing for contributions of mitochondrial DNA mutations to complex diseases

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Leber's disease and dystonia: a mitochondrial disease

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A SEX-LINKED HEREDO-DEGENERATIVE NEUROLOGICAL DISORDER ASSOCIATED WITH LEBER'S OPTIC ATROPHY. GENETICAL ASPECTS

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Maternal component in the familial aggregation of hypertension

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Leber's optic atrophy - an interdisciplinary study (author's transl)

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Leber's hereditary optic neuroretinopathy, a maternally inherited disease. A genealogic study in four pedigrees

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Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletion

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based on heuristic

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A mitochondrial DNA mutation as a cause of Leber's hereditary optic neuropathy

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12730827

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12 December 2020

based on heuristic

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Charcot-Marie-Tooth disease with Leber optic atrophy

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12 December 2020

based on heuristic

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Red cell glutathione in Leber's optic atrophy

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Mitochondrial DNA mutations in black Americans with hypertension-associated end-stage renal disease

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Identifiers

DOI

10.1086/375656

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12730827

retrieved

29 July 2017

PMC publication ID

1180311

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12730827

retrieved

29 July 2017

PubMed publication ID

12730827

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12730827

retrieved

29 July 2017

ResearchGate publication ID

10774169

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