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pro vyhledávání: '"Natalya F. Chipsanova"'
Publikováno v:
Вопросы современной педиатрии, Vol 21, Iss 6S, Pp 558-569 (2023)
Background. Fibrodysplasia ossificans progressiva (FOP) is a genetic disease of the heterotopic ossification group associated with the mutation in ACVR1/ALK2 gene. FOP is characterized by progressive heterotopic endochondral ossification of connectiv
Externí odkaz:
https://doaj.org/article/6529f25a20284d509c443c6e331b355a
