Familial Hyperekplexia, a Potential Cause of Cautious Gait: A New Korean Case and a Systematic Review of Phenotypes

Lee, Yoonju; Kim, Nan Young; Hong, Sangkyoon; Chung, Su Jin; Jeong, Seong Ho; Lee, Phil Hyu; Sohn, Young H

Lee, Yoonju; Kim, Nan Young; Hong, Sangkyoon; Chung, Su Jin; Jeong, Seong Ho; Lee, Phil Hyu; Sohn, Young H.

Afiliação

Lee Y; Department of Neurology, Yonsei University College of Medicine, Seoul, Korea.
Kim NY; Hallym Institute of Translational Genomics and Bioinformatics, Hallym University College of Medicine, Anyang, Korea.
Hong S; Hallym Institute of Translational Genomics and Bioinformatics, Hallym University College of Medicine, Anyang, Korea.
Chung SJ; Department of Neurology, Yonsei University College of Medicine, Seoul, Korea.
Jeong SH; Department of Neurology, Yonsei University College of Medicine, Seoul, Korea.
Lee PH; Department of Neurology, Yonsei University College of Medicine, Seoul, Korea.
Sohn YH; Department of Neurology, Yonsei University College of Medicine, Seoul, Korea.

J Mov Disord ; 10(1): 53-58, 2017 01.

Article em En | MEDLINE | ID: mdl-28122427

Palavras-chave

GLRA1; Hyperekplexia; deep phenotyping

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Systematic_reviews Idioma: En Revista: J Mov Disord Ano de publicação: 2017 Tipo de documento: Article

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