NR ALKF
AU 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.
TI Familial Creutzfeldt-Jakob disease with D178N-129M mutation of PRNP presenting as cerebellar ataxia without insomnia
QU Journal of Neurology, Neurosurgery and Psychiatry 2000 Mar; 68(3): 388
PT letter
MH Amyloid/*genetics; Cerebellar Ataxia/*diagnosis; Creutzfeldt-Jakob Syndrome/*diagnosis/*genetics; Diagnosis, Differential; Genotype; Human; Male; Middle Age; Mutation/*genetics; Pedigree; Protein Precursors/*genetics; Sleep Initiation and Maintenance Disorders/*diagnosis
SP englisch
PO England