Mutations in the nebulin gene can cause severe congenital nemaline myopathy-Reference-Cited by-同舟云学术

Mutations in the nebulin gene can cause severe congenital nemaline myopathy

Published:2002-10 Issue:7-8 Volume:12 Page:674-679
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Wallgren-Pettersson Carina,Donner Kati,Sewry Caroline,Bijlsma Emilia,Lammens Martin,Bushby Kate,Giovannucci Uzielli Maria Luisa,Lapi Elisabetta,Odent Sylvie,Akcoren Zuhal,Topaloğlu Haluk,Pelin Katarina

Publisher

Elsevier BV

Subject

Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health

Reference27 articles.

1. Workshop report: 40th ENMC international workshop: nemaline myopathy. 2–4 February 1996, Naarden, The Netherlands;Wallgren-Pettersson;Neuromusc Disord,1996

2. Clinical and genetic heterogeneity in autosomal recessive nemaline myopathy;Wallgren-Pettersson;Neuromusc Disord,1999

3. Report of the 70th ENMC International Workshop: nemaline myopathy;Wallgren-Pettersson;Neuromusc Disord,2000

4. A gene for autosomal recessive nemaline myopathy assigned to chromosome 2q by linkage analysis;Wallgren-Pettersson;Neuromusc Disord,1995

5. Refined localisation of the genes for nebulin and titin on chromosome 2q allows the assignment of nebulin as a candidate gene for autosomal recessive nemaline myopathy;Pelin;Eur J Hum Genet,1997

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