Novel Mutations Widen the Phenotypic Spectrum of Slow Skeletal/β-Cardiac Myosin (<i>MYH7</i>) Distal Myopathy
Laing early onset distal myopathy and myosin storage myopathy are caused by mutations of slow skeletal/β-cardiac myosin heavy chain encoded by the gene MYH7, as is a common form of familial hypertrophic/dilated cardiomyopathy. The mechanisms by which different phenotypes are produced by mutations in...
-д хадгалсан:
Үндсэн зохиолчид: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Формат: | Artigo |
Хэл сонгох: | англи |
Хэвлэсэн: |
2014
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Онлайн хандалт: | https://doi.org/10.1002/humu.22553 |
Шошгууд: |
Шошго нэмэх
Шошго байхгүй, Энэхүү баримтыг шошголох эхний хүн болох!
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