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Genetics of laminin α2 chain (or merosin) deficient congenital muscular dystrophy: from identification of mutations to prenatal diagnosis

✍ Scribed by Pascale Guicheney; Nicolas Vignier; Anne Helbling-Leclerc; Marja Nissinen; Xu Zhang; Corrinne Cruaud; Jean-Claude Lambert; Christian Richelme; Haluk Topaloglu; Luciano Merlini; Annie Barois; Ketty Schwartz; Fernando M.S. Tomé; Karl Tryggvason; Michel Fardeau


Book ID
117670702
Publisher
Elsevier Science
Year
1997
Tongue
English
Weight
667 KB
Volume
7
Category
Article
ISSN
0960-8966

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