A Pathogenic Presenilin-1 Val96Phe Mutation from a Malaysian Family.

Bagyinszky, Eva; Ch'ng, Gaik-Siew; Chan, Mei-Yan; An, Seong Soo A; Kim, SangYun

Bagyinszky, Eva; Ch'ng, Gaik-Siew; Chan, Mei-Yan; An, Seong Soo A; Kim, SangYun.

Afiliação

Bagyinszky E; Department of Industrial and Environmental Engineering, Graduate School of Environment, Gachon University, Seongnam 13120, Korea.
Ch'ng GS; Department of Genetics, Penang Hospital, Penang 10990, Malaysia.
Chan MY; Department of Genetics, Kuala Lumpur Hospital, Kuala Lumpur 50586, Malaysia.
An SSA; Department of Bionano Technology, Gachon University, Seongnam 13120, Korea.
Kim S; Department of Neurology, Seoul National University College of Medicine & Neurocognitive Behavior Center, Seoul National University Bundang Hospital, Seongnam 13620, Korea.

Brain Sci ; 11(10)2021 Oct 08.

Article em En | MEDLINE | ID: mdl-34679393

Palavras-chave

Alzheimer's disease; mutation; presenilin1; whole-exome sequencing

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Brain Sci Ano de publicação: 2021 Tipo de documento: Article

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