Homozygous LMNA mutation R527C in atypical Hutchinson-Gilford progeria syndrome: evidence for autosomal recessive inheritance. (Q47828931)

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scientific article published on 6 May 2009

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Language	Label	Description	Also known as
English	Homozygous LMNA mutation R527C in atypical Hutchinson-Gilford progeria syndrome: evidence for autosomal recessive inheritance.	scientific article published on 6 May 2009

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instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

19432833

retrieved

6 February 2018

reference URL

http://europepmc.org/abstract/MED/19432833

title

Homozygous LMNA mutation R527C in atypical Hutchinson-Gilford progeria syndrome: evidence for autosomal recessive inheritance. (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

19432833

retrieved

6 February 2018

reference URL

http://europepmc.org/abstract/MED/19432833

main subject

progeria

1 reference

based on heuristic

inferred from title

homozygosity

1 reference

based on heuristic

inferred from title

author name string

Lili Liang

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

19432833

retrieved

6 February 2018

reference URL

http://europepmc.org/abstract/MED/19432833

Huiwen Zhang

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

19432833

retrieved

6 February 2018

reference URL

http://europepmc.org/abstract/MED/19432833

Xuefan Gu

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

19432833

retrieved

6 February 2018

reference URL

http://europepmc.org/abstract/MED/19432833

language of work or name

English

0 references

publication date

6 May 2009

1 reference

stated in

Europe PubMed Central

PubMed publication ID

19432833

retrieved

6 February 2018

reference URL

http://europepmc.org/abstract/MED/19432833

published in

Acta Paediatrica

1 reference

stated in

Europe PubMed Central

PubMed publication ID

19432833

retrieved

6 February 2018

reference URL

http://europepmc.org/abstract/MED/19432833

volume

98

1 reference

stated in

Europe PubMed Central

PubMed publication ID

19432833

retrieved

6 February 2018

reference URL

http://europepmc.org/abstract/MED/19432833

issue

8

1 reference

stated in

Europe PubMed Central

PubMed publication ID

19432833

retrieved

6 February 2018

reference URL

http://europepmc.org/abstract/MED/19432833

page(s)

1365-1368

1 reference

stated in

Europe PubMed Central

PubMed publication ID

19432833

retrieved

6 February 2018

reference URL

http://europepmc.org/abstract/MED/19432833

cites work

Hutchinson-Gilford progeria syndrome: review of the phenotype.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1651-2227.2009.01324.X

retrieved

21 January 2018

Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome

1 reference

stated in

COCI

retrieved

24 May 2022

reference URL

https://opencitations.net/index/coci/api/v1/citations/10.1038/NATURE01629

Identifiers

DOI

10.1111/J.1651-2227.2009.01324.X

1 reference

stated in

Europe PubMed Central

PubMed publication ID

19432833

retrieved

6 February 2018

reference URL

http://europepmc.org/abstract/MED/19432833

PubMed publication ID

19432833

1 reference

stated in

Europe PubMed Central

PubMed publication ID

19432833

retrieved

6 February 2018

reference URL

http://europepmc.org/abstract/MED/19432833

 

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