Improvement of the diagnostic procedure in proximal myotonic myopathy/myotonic dystrophy type 2 (Q79357435)

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scientific article published on 10 December 2003

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Language	Label	Description	Also known as
English	Improvement of the diagnostic procedure in proximal myotonic myopathy/myotonic dystrophy type 2	scientific article published on 10 December 2003

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

14666402

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14666402%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 December 2019

title

Improvement of the diagnostic procedure in proximal myotonic myopathy/myotonic dystrophy type 2 (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

14666402

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14666402%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 December 2019

author name string

Sibylle Jakubiczka

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

14666402

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14666402%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 December 2019

Stefan Vielhaber

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

14666402

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14666402%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 December 2019

Wolfram Kress

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

14666402

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14666402%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 December 2019

Peter Küpferling

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

14666402

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14666402%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 December 2019

Ulrike Reuner

series ordinal

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

14666402

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14666402%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 December 2019

Bernhard Kunath

series ordinal

6

1 reference

stated in

Europe PubMed Central

PubMed publication ID

14666402

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14666402%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 December 2019

Peter Wieacker

series ordinal

7

1 reference

stated in

Europe PubMed Central

PubMed publication ID

14666402

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14666402%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 December 2019

publication date

10 December 2003

1 reference

stated in

Europe PubMed Central

PubMed publication ID

14666402

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14666402%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 December 2019

published in

Neurogenetics

1 reference

stated in

Europe PubMed Central

PubMed publication ID

14666402

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14666402%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 December 2019

volume

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

14666402

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14666402%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 December 2019

issue

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

14666402

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14666402%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 December 2019

page(s)

55-59

1 reference

stated in

Europe PubMed Central

PubMed publication ID

14666402

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14666402%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 December 2019

cites work

Proof of genetic heterogeneity in the proximal myotonic myopathy syndrome (PROMM) and its relationship to myotonic dystrophy type 2 (DM2)

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14666402

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14666402

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic mapping of a second myotonic dystrophy locus

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14666402

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14666402

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14666402

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14666402

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An unstable triplet repeat in a gene related to myotonic muscular dystrophy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14666402

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Myotonic dystrophy type 2: molecular, diagnostic and clinical spectrum

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14666402

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/S10048-003-0168-6

1 reference

stated in

Europe PubMed Central

PubMed publication ID

14666402

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14666402%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 December 2019

PubMed publication ID

14666402

1 reference

stated in

Europe PubMed Central

PubMed publication ID

14666402

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14666402%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 December 2019

 

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