Generalized Dystonia as a Cardinal Manifestation of Combined Oxidative Phosphorylation Deficiency 1.

Nayan, Aditya; Mehta, Shivangi; Chakravarty, Kamalesh; Mehta, Sahil; Lal, Vivek

Nayan, Aditya; Mehta, Shivangi; Chakravarty, Kamalesh; Mehta, Sahil; Lal, Vivek.

Afiliação

Nayan A; Department of Neurology, Post Graduate Institute of Medical Education and Research, Chandigarh, India.
Mehta S; Department of Psychiatry, Government Medical College and Hospital, Chandigarh, India.
Chakravarty K; Department of Neurology, Post Graduate Institute of Medical Education and Research, Chandigarh, India.
Mehta S; Department of Neurology, Post Graduate Institute of Medical Education and Research, Chandigarh, India.
Lal V; Department of Neurology, Post Graduate Institute of Medical Education and Research, Chandigarh, India.

Mov Disord Clin Pract ; 11(6): 742-745, 2024 Jun.

Article em En | MEDLINE | ID: mdl-38532288

Assuntos

Distonia; Humanos; Distonia/genética; Distonia/diagnóstico; Distonia/etiologia; Distúrbios Distônicos/genética; Distúrbios Distônicos/diagnóstico; Fosforilação Oxidativa

Palavras-chave

GFM1; combined oxidative phosphorylation deficiency; dystonia; mitochondria

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Distonia Limite: Humans Idioma: En Revista: Mov Disord Clin Pract / Mov. disord. clin. pract / Movement disorders clinical practice Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Índia

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