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pro vyhledávání: '"Homira Behbahani"'
Autor:
Mahmod Panahi, Patricia Rodriguez Rodriguez, Seyed-Mohammad Fereshtehnejad, Donia Arafa, Nenad Bogdanovic, Bengt Winblad, Angel Cedazo-Minguez, Juha Rinne, Taher Darreh-Shori, Yoshiki Hase, Raj N. Kalaria, Matti Viitanen, Homira Behbahani
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
Typical cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is caused by mutations in the human NOTCH3 gene. Cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy i
Externí odkaz:
https://doaj.org/article/f0ffe195729647bdadfe04bd8db3b90f