(Q53335969)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10838258%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

title

Report of the 70th ENMC International Workshop: nemaline myopathy, 11-13 June 1999, Naarden, The Netherlands (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10838258%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

0 references

1 reference

2

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10838258%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

author name string

C Wallgren-Pettersson

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10838258%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

publication date

1 June 2000

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10838258%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

published in

Neuromuscular Disorders

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10838258%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

volume

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10838258%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

page(s)

299-306

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10838258%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

issue

4-5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10838258%20AND%20SRC:MED&resulttype=core&format=json

Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathy

7 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900129-7

7 January 2021

Mutations in the nebulin gene associated with autosomal recessive nemaline myopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900129-7

7 January 2021

The complete primary structure of human nebulin and its correlation to muscle structure

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900129-7

7 January 2021

Myotilin, a novel sarcomeric protein with two Ig-like domains, is encoded by a candidate gene for limb-girdle muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900129-7

7 January 2021

A mutation in the alpha tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900129-7

7 January 2021

Homozygosity for a nonsense mutation in the alpha-tropomyosin slow gene TPM3 in a patient with severe infantile nemaline myopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900129-7

7 January 2021

Clinical and genetic heterogeneity in autosomal recessive nemaline myopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900129-7

7 January 2021

10.1016/S0960-8966(99)00129-7

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10838258%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

1 reference