Atypical phenotype in two patients with LAMA2 mutations-Reference-Cited by-同舟云学术

Atypical phenotype in two patients with LAMA2 mutations

Published:2014-05 Issue:5 Volume:24 Page:419-424
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Marques Joana,Duarte Sofia T.,Costa Sónia,Jacinto Sandra,Oliveira Jorge,Oliveira Márcia E.,Santos Rosário,Bronze-da-Rocha Elsa,Silvestre Ana Rita,Calado Eulália,Evangelista Teresinha

Publisher

Elsevier BV

Subject

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

Reference16 articles.

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2. LAMA2 gene analysis in a cohort of 26 congenital muscular dystrophy patients;Oliveira;Clin. Genet.,2008

3. Clinical and molecular study in congenital muscular dystrophy with partial laminin alpha 2 (LAMA2) deficiency;Tezak;Hum. Mutat.,2003

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

5. The dystrophin glycoprotein complex: signaling strength and integrity for the sarcolemma;Lapidos;Circ. Res.,2004

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