P097 A new locus for an autosomal recessive congenital muscular dystrophy without brain involvement maps to chromosome 7p21-Reference-Cited by-同舟云学术

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P097 A new locus for an autosomal recessive congenital muscular dystrophy without brain involvement maps to chromosome 7p21

Published:2009-09 Issue: Volume:13 Page:S51
ISSN:1090-3798
Container-title:European Journal of Paediatric Neurology
language:en
Short-container-title:European Journal of Paediatric Neurology

Author:

Cirak S.,Herrmann R.,Ruthland P.,Brockmann K.,Korinthenberg R.,Nürnberg P.,Muntoni F.,Voit T.

Publisher

Elsevier BV

Subject

Neurology (clinical),General Medicine,Pediatrics, Perinatology and Child Health

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Case Report: ISPD Gene Mutation Leads to Dystroglycanopathies: Genotypic Phenotype Analysis and Treatment Exploration;Frontiers in Pediatrics;2021-08-18

2. A novel homozygous ISPD gene mutation causing phenotype variability in a consanguineous family;Neuromuscular Disorders;2015-01

3. ISPD gene mutations are a common cause of congenital and limb-girdle muscular dystrophies;Brain;2013-01-01

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