Clinical and genetic characteristics of congenital muscular dystrophies (Part 1)

Congenital muscular dystrophy is an extremely heterogeneous group of hereditary neuromuscular diseases that are clinically characterized by muscular hypotonia, progressive muscle weakness, and dystrophic changes in the muscles. Overlapping clinical symptoms and many genes that have to be analyzed to...

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Bibliographic Details
Main Authors: P. A. Chausova, O. P. Ryzhkova, A. V. Polyakov
Format: Article
Language:Russian
Published: ABV-press 2020-06-01
Series:Нервно-мышечные болезни
Subjects:
Online Access:https://nmb.abvpress.ru/jour/article/view/369
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