Familial Creutzfeldt-Jakob disease with D178N-129M mutation of PRNP presenting as cerebellar ataxia without insomnia

Por TANIWAKI, Y, HARA, H, DOH-URA, K, MURAKAMI, I, TASHIRO, H, YAMASAKI, T, SHIGETO, H, ARAKAWA, K, ARAKI, E, YAMADA, T, IWAKI, T, KIRA, J
Publicado em 2000