Founder mutation causes classical Fukuyama congenital muscular dystrophy (FCMD) in Chinese patients-Reference-Cited by-同舟云学术

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Founder mutation causes classical Fukuyama congenital muscular dystrophy (FCMD) in Chinese patients

Published:2015-10 Issue:9 Volume:37 Page:880-886
ISSN:0387-7604
Container-title:Brain and Development
language:en
Short-container-title:Brain and Development

Author:

Yang Haipo,Kobayashi Kazuhiro,Wang Shuo,Jiao Hui,Xiao Jiangxi,Toda Tatsushi,Wu Xiru,Xiong Hui

Funder

National Natural Science Foundation of China

National Basic Research Program of China

Publisher

Elsevier BV

Subject

Neurology (clinical),Developmental Neuroscience,General Medicine,Pediatrics, Perinatology and Child Health

Reference22 articles.

1. A genetic study of the Fukuyama type congenital muscular dystrophy;Fukuyama;Brain Dev,1984

2. Congenital progressive muscular dystrophy of the Fukuyama types – clinical, genetic and pathological considerations;Fukuyama;Brain Dev,1981

3. Saito, K. Fukuyama Congenital Muscular Dystrophy. GeneReviews Last Update: May 10; 2012.

4. Peripheral nerve involvement in Fukuyama congenital muscular dystrophy: a case report;Jang;J Child Neurol,2013

5. Founder SVA retrotransposal insertion in Fukuyama-type congenital muscular dystrophy and its origin in Japanese and Northeast Asian populations;Watanabe;Am J Med Genet A,2005

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