Dystrophin gene analysis in Hungarian Duchenne/Becker muscular dystrophy families – Detection of carrier status in symptomatic and asymptomatic female relatives-Reference-Cited by-同舟云学术

Dystrophin gene analysis in Hungarian Duchenne/Becker muscular dystrophy families – Detection of carrier status in symptomatic and asymptomatic female relatives

Published:2009-02 Issue:2 Volume:19 Page:108-112
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Pikó Henriett,Vancsó Viktor,Nagy Bálint,Bán Zoltán,Herczegfalvi Ágnes,Karcagi Veronika

Publisher

Elsevier BV

Subject

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

Reference42 articles.

1. The dystrophin-associated protein complex;Ehmsen;J Cell Sci,2002

2. Dystrophin, its gene, and the dystrophinopathies;Roberts;Adv Genet,1995

3. Dystrophin: the protein product of the Duchenne muscular dystrophy locus;Hoffman;Cell,1987

4. The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein;Koenig;Cell,1988

5. Topography of the Duchenne muscular dystrophy 8d0d9 gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications;Den-Dunnen;Am J Hum Genet,1999

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