Heterozygous YY1 mutation - A mimicker of SGCE-myoclonus-dystonia.

Chawla, Tanushree; Kumar, Natasha K; Goyal, Vinay

Chawla, Tanushree; Kumar, Natasha K; Goyal, Vinay.

Affiliation

Chawla T; Department of Neurology, Institute of Neurosciences, Medanta, The Medicity, Gurugram, Haryana, India.
Kumar NK; Consultant Clinical Neuropsychologist, Institute of Neurosciences, Medanta, The Medicity, Gurugram, Haryana, India.
Goyal V; Department of Neurology, Institute of Neurosciences, Medanta, The Medicity, Gurugram, Haryana, India. Electronic address: drvinaygoyal@gmail.com.

Parkinsonism Relat Disord ; 117: 105846, 2023 Dec.

Article in En | MEDLINE | ID: mdl-37690905

Subject(s)

Dystonic Disorders; Myoclonus; Humans; Dystonic Disorders/diagnosis; Dystonic Disorders/genetics; Mutation/genetics; Heterozygote; Sarcoglycans/genetics; Myoclonus/genetics; YY1 Transcription Factor/genetics

Key words

Dystonia; Gabriele de vries syndrome; Writers cramp; YY1 mutation

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Full text: 1 Database: MEDLINE Main subject: Dystonic Disorders / Myoclonus Language: En Journal: Parkinsonism Relat Disord Year: 2023 Type: Article Affiliation country: India

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