Changes of laminin β2 chain expression in congenital muscular dystrophy
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health
Reference31 articles.
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2. Congenital muscular dystrophy with merosin deficiency;Tomé;C R Acad Scí Paris, Life Sci.,1994
3. Expression of laminin subunits in congenital muscular dystrophy;Sewry;Neuromusc Disord,1995
4. Localization of merosin negative congenital muscular dystrophy to chromosome 6q2 by homozygosity mapping;Hillaire;Human Mol Genet,1994
5. Mutations in the laminin α-2 chain gene (LAMA2) cause merosin deficient congenital muscular dystrophy;Helbling-Leclerc;Nature Genet,1995
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