Familial Creutzfeldt-Jakob disease with D178N-129M mutation of PRNP presenting as cerebellar ataxia without insomnia
Y. Taniwaki, H. Hara, K. Doh-Ura, I. Murakami, H. Tashiro, T. Yamasaki, H. Shigeto, K. Arakawa, E. Araki, T. Yamada, T. Iwaki, J. Kira
研究成果: Letter › 査読
32
被引用数
(Scopus)