Mutations in the laminin α2–chain gene (LAMA2) cause merosin–deficient congenital muscular...

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© 1995 Nature Publishing Group http://www.nature.com/naturegenetics

Transcript of Mutations in the laminin α2–chain gene (LAMA2) cause merosin–deficient congenital muscular...

Page 1: Mutations in the laminin α2–chain gene (LAMA2) cause merosin–deficient congenital muscular dystrophy

© 1995 Nature Publishing Group http://www.nature.com/naturegenetics

Page 2: Mutations in the laminin α2–chain gene (LAMA2) cause merosin–deficient congenital muscular dystrophy

© 1995 Nature Publishing Group http://www.nature.com/naturegenetics

Page 3: Mutations in the laminin α2–chain gene (LAMA2) cause merosin–deficient congenital muscular dystrophy

© 1995 Nature Publishing Group http://www.nature.com/naturegenetics


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Muscular Dystrophy

Muscular Dystrophy

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Laminin-8 and lymphoid cells - pdfs.semanticscholar.org€¦ · Accordingly, laminin-8 and laminin-10/11, but not laminin-1, strongly costimulated proliferation of the T cells via

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Clinical, genetic, and structural basis of congenital …Clinical, genetic, and structural basis of congenital adrenal hyperplasia due to 11β-hydroxylase deficiency Ahmed Khattaba,b,1,2,

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