Author:
Specht Sabine,Duff Jennifer,Charlton Richard,Polvikoski Tuomo,Barresi Rita,Töpf Ana,Straub Volker
Funder
Seventh Framework Programme
Subject
Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health
Reference27 articles.
1. Bridging structure with function: structural, regulatory, and developmental role of laminins;Tzu;Int J Biochem Cell Biol,2008
2. Merosin/laminin-2 and muscular dystrophy;Wewer;Neuromuscul Disord,1996
3. Laminins in basement membrane assembly;Hohenester;Cell Adhes Migr,2013
4. Genotype-phenotype correlation in a large population of muscular dystrophy patients with LAMA2 mutations;Geranmayeh;Neuromuscul Disord,2010
5. Merosin-deficient congenital muscular dystrophy, autosomal recessive (MDC1A, MIM#156225, LAMA2 gene coding for α2 chain of laminin);Allamand;Eur J Hum Genet,2002
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