A new mutation of the SCGA gene is the cause of a late onset mild phenotype limb girdle muscular dystrophy type 2D with axial involvement-Reference-Cited by-同舟云学术

A new mutation of the SCGA gene is the cause of a late onset mild phenotype limb girdle muscular dystrophy type 2D with axial involvement

Published:2018-08 Issue:8 Volume:28 Page:633-638
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Gonzalez-Quereda Lidia^ORCID,Gallardo Eduard,Töpf Ana,Alonso-Jimenez Alicia,Straub Volker^ORCID,Rodriguez Maria Jose,Lleixa Cinta,Illa Isabel,Gallano Pia^ORCID,Diaz-Manera Jordi

Publisher

Elsevier BV

Subject

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

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4. Sarcoglycanopathies;Kirschner;Handb Clin Neurol,2011

5. Sarcoglycanopathies in Dutch patients with autosomal recessive limb girdle muscular dystrophy;Ginjaar;J Neurol,2000

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