Genotype–phenotype correlation in a large population of muscular dystrophy patients with LAMA2 mutations-Reference-Cited by-同舟云学术

Genotype–phenotype correlation in a large population of muscular dystrophy patients with LAMA2 mutations

Published:2010-04 Issue:4 Volume:20 Page:241-250
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Geranmayeh Fatemeh,Clement Emma,Feng Lucy H,Sewry Caroline,Pagan Judith,Mein Rachael,Abbs Stephen,Brueton Louise,Childs Anne-Marie,Jungbluth Heinz,De Goede Christian G,Lynch Bryan,Lin Jean-Pierre,Chow Gabriel,Sousa Carlos de,O’Mahony Olivia,Majumdar Anirban,Straub Volker,Bushby Katherine,Muntoni Francesco

Publisher

Elsevier BV

Subject

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

Reference47 articles.

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4. Congenital muscular dystrophy associated with merosin deficiency;North;J Child Neurol,1996

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

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