Zobrazeno 1 - 1
of 1
pro vyhledávání: '"Nuno Álvaro Silva"'
Publikováno v:
BMC Ophthalmology, Vol 24, Iss 1, Pp 1-6 (2024)
Abstract Background Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation is a rare autosomal dominant disease caused by mutations in KIF11 which disrupt EG5 protein function, impacting the development and maintenance of r
Externí odkaz:
https://doaj.org/article/e9c9f5dbb8bb4065b273fd2d4f7ecf6f
