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

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Bibliographic Details
Published in:Journal of neurology, neurosurgery and psychiatry neurosurgery and psychiatry, 2000-03, Vol.68 (3), p.388-388
Main Authors: 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
Format: Article
Language:English
Subjects:
Amyloid - genetics
Cerebellar Ataxia - diagnosis
Creutzfeldt-Jakob Syndrome - diagnosis
Creutzfeldt-Jakob Syndrome - genetics
Diagnosis, Differential
Genotype
Humans
Letters to the Editor
Male
Middle Aged
Mutation - genetics
Pedigree
Prion Proteins
Prions
Protein Precursors - genetics
Sleep Initiation and Maintenance Disorders - diagnosis
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ISSN:0022-3050
1468-330X
DOI:10.1136/jnnp.68.3.388