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pro vyhledávání: '"Mostafa Rayati"'
Publikováno v:
Journal of Pediatrics Review, Vol 8, Iss 1, Pp 35-46 (2020)
Introduction: Laing early-onset distal myopathy is a disorder with autosomal dominant inheritance pattern caused by a mutation in the MYH7 gene that encodes the human β-myosin heavy chain. Most previous studies reported this disorder with mild sympt
Externí odkaz:
https://doaj.org/article/5dc14608323b464db203bfe84e69d05b
Publikováno v:
Journal of Pediatrics Review, Vol 8, Iss 1, Pp 35-46 (2020)
Introduction: Laing early-onset distal myopathy is a disorder with autosomal dominant inheritance pattern caused by a mutation in the MYH7 gene that encodes the human β-myosin heavy chain. Most previous studies reported this disorder with mild sympt