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Mutations in the slow skeletal muscle fiber myosin heavy chain gene (MYH7) cause Laing Early-Onset distal myopathy (MPD1)
Journal article   Peer reviewed

Mutations in the slow skeletal muscle fiber myosin heavy chain gene (MYH7) cause Laing Early-Onset distal myopathy (MPD1)

C. Meredith, R. Herrmann, C. Parry, K. Liyanage, D.E. Dye, H.J. Durling, R.M. Duff, K. Beckman, M. de Visser, M.M. van der Graaff, …
The American Journal of Human Genetics, Vol.75(4), pp.703-708
2004
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Abstract

We previously linked Laing-type early-onset autosomal dominant distal myopathy (MPD1) to a 22-cM region of chromosome 14. One candidate gene in the region, MYH7, which is mutated in cardiomyopathy and myosin storage myopathy, codes for the myosin heavy chain of type I skeletal muscle fibers and cardiac ventricles...

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Collaboration types
Domestic collaboration
International collaboration
Citation topics
1 Clinical & Life Sciences
1.96 Cell Biology
1.96.492 Myosin
Web Of Science research areas
Genetics & Heredity
ESI research areas
Molecular Biology & Genetics
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