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pro vyhledávání: '"Zafar Maasoumi Moghaddam"'
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 23, Iss 1, Pp 1-5 (2022)
Abstract Introduction Ullrich congenital muscular dystrophy (UCMD) is a severe form of inherited muscle weakness at birth. Recent genetic studies discovered that different gene mutations are responsible for UCMD clinical manifestation. Case report In
Externí odkaz:
https://doaj.org/article/9ea5f510e6a2451cb4c0efce70df56d2