Familial Creutzfeldt-Jakob disease with a mutation at codon 180 presenting with an atypical phenotype.

Yeo, Min-Ju; Lee, Seung-Hwan; Lee, Seo-Young; Jeon, Yong-Chul; Park, Seok-Joo; Cho, Han-Jeong; Choi, Kyoung-Chan; Kim, Yong-Sun; Kim, Sung-Hun

Yeo, Min-Ju; Lee, Seung-Hwan; Lee, Seo-Young; Jeon, Yong-Chul; Park, Seok-Joo; Cho, Han-Jeong; Choi, Kyoung-Chan; Kim, Yong-Sun; Kim, Sung-Hun.

Affiliation

Yeo MJ; Department of Neurology, School of Medicine, Kangwon National University, Hyoja 3-dong, Chuncheon, Kangwon-do 200-947, Republic of Korea.

J Clin Neurosci ; 20(1): 180-2, 2013 Jan.

Article in En | MEDLINE | ID: mdl-22999564

Subject(s)

Codon/genetics; Creutzfeldt-Jakob Syndrome/genetics; Mutation/genetics; Prions/genetics; Aged; Female; Humans; Phenotype; Valine/genetics

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prions / Codon / Creutzfeldt-Jakob Syndrome / Mutation Limits: Aged / Female / Humans Language: En Journal: J Clin Neurosci Journal subject: NEUROLOGIA Year: 2013 Document type: Article Country of publication: United kingdom

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