APA

Kamimura K., Takahashi K., Uyama E., Tokunaga M., Kotorii S., Uchino M. & Tabira T. (20000118). Identification of a Notch3 mutation in a Japanese CADASIL family. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. : Alzheimer disease and associated disorders.

Chicago

Kamimura K, Takahashi K, Uyama E, Tokunaga M, Kotorii S, Uchino M and Tabira T. 20000118. Identification of a Notch3 mutation in a Japanese CADASIL family. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. : Alzheimer disease and associated disorders.

Harvard

Kamimura K., Takahashi K., Uyama E., Tokunaga M., Kotorii S., Uchino M. and Tabira T. (20000118). Identification of a Notch3 mutation in a Japanese CADASIL family. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. : Alzheimer disease and associated disorders.

MLA

Kamimura K, Takahashi K, Uyama E, Tokunaga M, Kotorii S, Uchino M and Tabira T. Identification of a Notch3 mutation in a Japanese CADASIL family. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. : Alzheimer disease and associated disorders. 20000118.