Results
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5510.
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5511.
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Familial Creutzfeldt-Jakob disease with D178N-129M mutation of PRNP presenting as cerebellar ataxia without insomnia. [electronic resource] by
- 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
Producer: 20000421
In:
Journal of neurology, neurosurgery, and psychiatry vol. 68
Availability: No items available.
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