Merosin-positive congenital muscular dystrophy with transient brain dysmyelination, pontocerebellar hypoplasia and mental retardation
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health
Reference38 articles.
1. Congenital muscular dystrophy with merosin deficiency;Tomé;C R Acad Sci Paris, Life Sci,1994
2. Localization of merosin negative congenital muscular dystrophy to chromosome 6q2 by homozygosity mapping;Hillaire;Hum Mol Genet,1994
3. Mutations in the laminin α2 chain gene (LAMA2) cause merosin deficient congenital muscular dystrophy;Helbling-Leclerc;Nat Genet,1995
4. A peculiar form of congenital muscular dystrophy;Fukuyama;Paediatr Universit Tokyo,1960
5. Localisation of a gene for Fukuyama type congenital muscular dystrophy to chromosome 9q31–33;Toda;Nat Genet,1993
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