Infantile facioscapulohumeral muscular dystrophy revisited: Expansion of clinical phenotypes in patients with a very short EcoRI fragment-Reference-Cited by-同舟云学术

Infantile facioscapulohumeral muscular dystrophy revisited: Expansion of clinical phenotypes in patients with a very short EcoRI fragment

Published:2013-04 Issue:4 Volume:23 Page:298-305
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Chen Tai-Heng,Lai Yu-Hung,Lee Pei-Lun,Hsu Jong-Hau,Goto Kanako,Hayashi Yukiko K.,Nishino Ichizo,Lin Chin-Wen,Shih Hsiang-Hung,Huang Chao-Ching,Liang Wen-Chen,Wang Wen-Fu,Jong Yuh-Jyh

Publisher

Elsevier BV

Subject

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

Reference31 articles.

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4. Facioscapulohumeral muscular dystrophy: clinical diversity and genetic abnormalities in Japanese patients;Nakagawa;Intern Med,1997

5. Facioscapulohumeral muscular dystrophy: hearing loss and other atypical features of patients with large 4q35 deletions;Trevisan;Eur J Neurol,2008

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