Possible Role of a Missense Mutation of p.P167S on <i>NOTCH3</i> Gene Associated with Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy.

Choi, Byung Woo; Park, Seongho; Kim, Hee-Jin

Possible Role of a Missense Mutation of p.P167S on NOTCH3 Gene Associated with Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy.

Choi, Byung Woo; Park, Seongho; Kim, Hee-Jin.

Afiliação

Choi BW; Department of Neurology, College of Medicine, Hanyang University, Seoul, Korea.
Park S; Department of Neurology, College of Medicine, Hanyang University, Seoul, Korea.
Kim HJ; Department of Neurology, College of Medicine, Hanyang University, Seoul, Korea.

Dement Neurocogn Disord ; 15(2): 52-54, 2016 Jun.

Article em En | MEDLINE | ID: mdl-30906341

Palavras-chave

c.499C>T; cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy; p.P167S

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Revista: Dement Neurocogn Disord Ano de publicação: 2016 Tipo de documento: Article País de publicação:

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