Extramuscular manifestations in children with severe congenital myopathy due to ACTA1 gene mutations-Reference-Cited by-同舟云学术

Extramuscular manifestations in children with severe congenital myopathy due to ACTA1 gene mutations

Published:2011-07 Issue:7 Volume:21 Page:489-493
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Saito Yoshiaki,Komaki Hirofumi,Hattori Ayako,Takeuchi Fumi,Sasaki Masayuki,Kawabata Ken,Mitsuhashi Satomi,Tominaga Kayo,Hayashi Yukiko K.,Nowak Kristen J.,Laing Nigel G.,Nonaka Ikuya,Nishino Ichizo

Publisher

Elsevier BV

Subject

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

Reference15 articles.

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2. Mucle disease caused by mutations in the skeletal muscle alpha-actin gene (ACTA1);Sparrow;Neuromuscul Disord,2003

3. Mutations and polymorphisms of the skeletal muscle alpha-actin gene (ACTA1);Laing;Hum Mutat,2009

4. Zebra body myopathy resolved;Sewry;Neuromuscul Disord,2009

5. Nemaline (actin) myopathy with myofibrillar dysgenesis and abnormal ossification;Arai;Neuromuscul Disord,2009

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