Zobrazeno 1 - 1
of 1
pro vyhledávání: '"Mina Mısırlıgil"'
Publikováno v:
JCRPE, Vol 13, Iss 4, Pp 452-455 (2021)
Kabuki syndrome (KS) is a disease characterized by distinctive facial features, skeletal anomalies and delay in neuromotor development. KS 1 is an autosomal dominant condition caused by mutations in the KMT2D gene, whereas KS 2 is an X-linked disorde
Externí odkaz:
https://doaj.org/article/027c57406003485e89453a93e2924fd3
