RT Journal Article
SR Electronic
T1 Familial Creutzfeldt-Jakob disease with D178N-129M mutation of<em>PRNP</em> presenting as cerebellar ataxia without insomnia
JF Journal of Neurology, Neurosurgery &amp; Psychiatry
JO J Neurol Neurosurg Psychiatry
FD BMJ Publishing Group Ltd
SP 388
OP 388
DO 10.1136/jnnp.68.3.388
VO 68
IS 3
A1 Y TANIWAKI
A1 H HARA
A1 K DOH-URA
A1 I MURAKAMI
A1 H TASHIRO
A1 T YAMASAKI
A1 H SHIGETO
A1 K ARAKAWA
A1 E ARAKI
A1 T YAMADA
A1 T IWAKI
A1 J KIRA
YR 2000
UL http://jnnp.bmj.com/content/68/3/388.1.abstract
AB