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J Neurol Sci. 2015 May 15;352(1-2):108-9. doi: 10.1016/j.jns.2015.03.017. Epub 2015 Mar 19.

Creutzfeldt-Jakob disease with homozygous M232R mutation: A case report.

Author information

1
Department of Neurology, Aomori Prefectural Central Hospital, Aomori, Japan; Department of Neuropathology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan. Electronic address: t-kon@umin.ac.jp.
2
Department of Neurology, Aomori Prefectural Central Hospital, Aomori, Japan; Department of Neuropathology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
3
Department of Neurology, Aomori Prefectural Central Hospital, Aomori, Japan.
4
Department of Neurology, Aomori Hospital, Aomori, Japan.
5
Aoba Neurosurgical Clinic, Sendai, Japan.
6
Department of Neurological Science, Tohoku University Graduate School of Medicine, Sendai, Japan.

KEYWORDS:

Creutzfeldt–Jakob disease; Homozygous mutation; M232R; Polymorphism; Prion protein gene; Substitution

PMID:
25818675
DOI:
10.1016/j.jns.2015.03.017
[Indexed for MEDLINE]

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