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Mutations in the slow skeletal muscle fiber myosin heavy chain gene (MYH7) cause Laing Early-Onset distal myopathy (MPD1)
- Source :
- Meredith, C., Herrmann, R., Parry, C., Liyanage, K., Dye, D.E., Durling, H.J., Duff, R.M., Beckman, K., de Visser, M., van der Graaff, M.M., Hedera, P., Fink, J.K., Petty, E.M., Lamont, P., Fabian, V., Bridges, L., Voit, T., Mastaglia, F.L. <
- Publication Year :
- 2004
-
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...
Details
- Database :
- OAIster
- Journal :
- Meredith, C., Herrmann, R., Parry, C., Liyanage, K., Dye, D.E., Durling, H.J., Duff, R.M., Beckman, K., de Visser, M., van der Graaff, M.M., Hedera, P., Fink, J.K., Petty, E.M., Lamont, P., Fabian, V., Bridges, L., Voit, T., Mastaglia, F.L. <
- Notes :
- English
- Publication Type :
- Electronic Resource
- Accession number :
- edsoai.ocn907440642
- Document Type :
- Electronic Resource