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pro vyhledávání: '"Jacquelyn Olavarria"'
Publikováno v:
Stem Cell Research & Therapy, Vol 11, Iss 1, Pp 1-15 (2020)
Abstract Background Congenital muscular dystrophies (CMD) are a clinically and genetically heterogeneous group of neuromuscular disorders characterized by muscle weakness. The two most prevalent forms of CMD, collagen VI-related myopathies (COL6RM) a
Externí odkaz:
https://doaj.org/article/85d15c56570f41bba25bbfcd88db61c6
