Genotype/phenotype analysis in Chinese laminin-α2 deficient congenital muscular dystrophy patients-Reference-Cited by-同舟云学术

Genotype/phenotype analysis in Chinese laminin-α2 deficient congenital muscular dystrophy patients

Published:2014-03-31 Issue:3 Volume:87 Page:233-243
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Xiong H.¹,Tan D.¹,Wang S.¹,Song S.²,Yang H.¹,Gao K.¹,Liu A.¹,Jiao H.¹,Mao B.³,Ding J.¹,Chang X.¹,Wang J.¹,Wu Y.¹,Yuan Y.⁴,Jiang Y.¹,Zhang F.⁵,Wu H.⁶,Wu X.¹

Affiliation:

1. Department of Pediatrics; Peking University First Hospital; Beijing China

2. Department of Medical Genetics, School of Basic Medical Sciences; Peking University; Beijing China

3. Department of Neurology; Wuhan Children's Hospital; Wuhan China

4. Department of Neurology; Peking University First Hospital; Beijing China

5. School of Life Sciences; Fudan University; Shanghai China

6. Department of Neurology; Beijing Children's Hospital; Beijing China

Funder

the National Natural Science Foundation of China

the National Basic Research Program of China

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference18 articles.

1. Clinical phenotype in congenital muscular dystrophy: correlation with expression of merosin in skeletal muscle;Philpot;Neuromuscul Disord,1995

2. Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy;Hellbling-Ledlerc;Nat Genet,1995

3. Laminin alpha2 muscular dystrophy: genotype/phenotype studies of 22 patients;Pegoraro;Neurology,1998

4. Genotype-phenotype correlation in a large population of muscular dystrophy patients with LAMA2 mutations;Geranmayeh;Neuromuscul Disord,2010

5. Form and function: the laminin family of heterotrimers;Colognato;Dev Dyn,2000

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