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Human Molecular Genetics|September 26, 1997

Mutations in the MTM1 gene implicated in X-linked myotubular myopathy. ENMC International Consortium on Myotubular Myopathy. European Neuro-Muscular CenterJ Laporte, C Guiraud-Chaumeil, M C Vincent, et al.

Neuromuscular Disorders : NMD|March 21, 2001

Nebulin expression in patients with nemaline myopathyJ Gurgel-Giannetti, U Reed, M L Bang, et al.

Proceedings of the National Academy of Sciences of the United States of America|March 3, 1999

Mutations in the nebulin gene associated with autosomal recessive nemaline myopathyK Pelin, P Hilpelä, K Donner, et al.

Neuromuscular Disorders : NMD|January 5, 2000

Clinical and genetic heterogeneity in autosomal recessive nemaline myopathyC Wallgren-Pettersson, K Pelin, P Hilpelä, et al.

Nature Genetics|October 3, 1999

Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathyK J Nowak, D Wattanasirichaigoon, H H Goebel, et al.

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Showing results (31-40 of 35) with videos related to

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You have reached the last page of results.This site can display upto 35 results.

Human Molecular Genetics|September 26, 1997

Mutations in the MTM1 gene implicated in X-linked myotubular myopathy. ENMC International Consortium on Myotubular Myopathy. European Neuro-Muscular CenterJ Laporte, C Guiraud-Chaumeil, M C Vincent, et al.

Neuromuscular Disorders : NMD|March 21, 2001

Nebulin expression in patients with nemaline myopathyJ Gurgel-Giannetti, U Reed, M L Bang, et al.

Proceedings of the National Academy of Sciences of the United States of America|March 3, 1999

Mutations in the nebulin gene associated with autosomal recessive nemaline myopathyK Pelin, P Hilpelä, K Donner, et al.

Neuromuscular Disorders : NMD|January 5, 2000

Clinical and genetic heterogeneity in autosomal recessive nemaline myopathyC Wallgren-Pettersson, K Pelin, P Hilpelä, et al.

Nature Genetics|October 3, 1999

Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathyK J Nowak, D Wattanasirichaigoon, H H Goebel, et al.

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