LAMA2 gene analysis in a cohort of 26 congenital muscular dystrophy patients-Reference-Cited by-同舟云学术

LAMA2 gene analysis in a cohort of 26 congenital muscular dystrophy patients

Published:2008-08-12 Issue:6 Volume:74 Page:502-512
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Oliveira J,Santos R,Soares-Silva I,Jorge P,Vieira E,Oliveira ME,Moreira A,Coelho T,Ferreira JC,Fonseca MJ,Barbosa C,Prats J,Aríztegui ML,Martins ML,Moreno T,Heinimann K,Barbot C,Pascual-Pascual SI,Cabral A,Fineza I,Santos M,Bronze-da-Rocha E

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2008.01068.x/fullpdf

Reference23 articles.

1. Congenital muscular dystrophy with merosin deficiency;Tomé;C R Acad Sci III,1994

2. Genetic epidemiology of congenital muscular dystrophy in a sample from north-east Italy;Mostacciuolo;Hum Genet,1991

3. Merosin and congenital muscular dystrophy;Miyagoe-Suzuki;Microsc Res Tech,2000

4. The congenital muscular dystrophies: recent advances and molecular insights;Mendell;Pediatr Dev Pathol,2006

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

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