Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Masafumi Ihara"'
Autor:
Yumi Yamamoto, Katsutoshi Kojima, Daisuke Taura, Masakatsu Sone, Kazuo Washida, Naohiro Egawa, Takayuki Kondo, Eiko N. Minakawa, Kayoko Tsukita, Takako Enami, Hidekazu Tomimoto, Toshiki Mizuno, Raj N. Kalaria, Nobuya Inagaki, Ryosuke Takahashi, Mariko Harada-Shiba, Masafumi Ihara, Haruhisa Inoue
Publikováno v:
Molecular Brain, Vol 13, Iss 1, Pp 1-12 (2020)
Abstract Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is one of the most common forms of hereditary cerebral small vessel diseases and is caused by mutations in NOTCH3. Our group has previously
Externí odkaz:
https://doaj.org/article/b9af76ea335a4855af63285e62998857
Autor:
Nobuya Inagaki, Masafumi Ihara, Toshiki Mizuno, Masakatsu Sone, Raj N. Kalaria, Yamamoto Yumi, Katsutoshi Kojima, Ryosuke Takahashi, Eiko N. Minakawa, Takako Enami, Hidekazu Tomimoto, Kayoko Tsukita, Kazuo Washida, Haruhisa Inoue, Mariko Harada-Shiba, Daisuke Taura, Naohiro Egawa, Takayuki Kondo
Publikováno v:
Molecular Brain, Vol 13, Iss 1, Pp 1-12 (2020)
Molecular Brain
Molecular Brain
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is one of the most common forms of hereditary cerebral small vessel diseases and is caused by mutations in NOTCH3. Our group has previously reported