Correlation between muscle involvement, phenotype and D4Z4 fragment size in facioscapulohumeral muscular dystrophy-Reference-Cited by-同舟云学术

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Correlation between muscle involvement, phenotype and D4Z4 fragment size in facioscapulohumeral muscular dystrophy

Published:2012-04 Issue:4 Volume:22 Page:331-338
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Wang Chien-Hua,Leung Mana,Liang Wen-Chen,Hsieh Tysh-Jyi,Chen Tai-Heng,Jong Yuh-Jyh

Publisher

Elsevier BV

Subject

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

Reference20 articles.

1. Facioscapulohumeral muscular dystrophy: a clinician’s experience;Padberg,2004

2. Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy;Wijmenga;Nat Genet,1992

3. Fascioscapulohumeral dystrophy;Kissel;Semin Neurol,1999

4. The D4Z4 repeat-mediated pathogenesis of facioscapulohumeral muscular dystrophy;Van der Maarel;Am J Hum Genet,2005

5. Profiles of neuromuscular diseases. Facioscapulohumeral muscular dystrophy;Kilmer;Am J Phys Med Rehabil,1995

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