Mutations in the laminin α2–chain gene (LAMA2) cause merosin–deficient congenital muscular dystrophy
A. Leclerc(Pitié-Salpêtrière Hospital), Xu Zhang(University of Oulu), Haluk Topaloğlu(Hacettepe University Hospital), Corinne Cruaud(Genethon (France)), Frédérique Tesson(Inserm), Jean Weissenbach(Genethon (France)), F.M.S. Tomé(Inserm), Ketty Schwartz(Sorbonne Université), Michel Fardeau(Inserm), Karl Tryggvason(University of Oulu), Pascale Guicheney(Sorbonne Université)
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