Genotype-phenotype analysis in X-linked Emery–Dreifuss muscular dystrophy and identification of a missense mutation associated with a milder phenotype-Reference-Cited by-同舟云学术

Genotype-phenotype analysis in X-linked Emery–Dreifuss muscular dystrophy and identification of a missense mutation associated with a milder phenotype

Published:1999-05 Issue:3 Volume:9 Page:159-165
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Yates John R.W,Bagshaw Jane,Aksmanovic Veronica M.A,Coomber Ellen,McMahon Robert,Whittaker Joanne L,Morrison Patrick J,Kendrick-Jones John,Ellis Juliet A

Publisher

Elsevier BV

Subject

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

Reference33 articles.

1. Emery–Dreifuss syndrome;Emery;J Med Genet,1989

2. Identification of a novel X-linked gene responsible for Emery–Dreifuss muscular dystrophy;Bione;Nat Genet,1994

3. Emerin deficiency at the nuclear membrane in patients with Emery–Dreifuss muscular dystrophy;Nagano;Nat Genet,1996

4. The Emery–Dreifuss muscular dystrophy protein, emerin, is a nuclear membrane protein;Manilal;Hum Mol Genet,1996

5. Linkage studies in Emery–Dreifuss muscular dystrophy;Paquis;J Genet Hum,1989

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