Dysarthria, Ataxia, and Dystonia Associated with <i>COX20 (FAM36A)</i> Gene Mutation: A Case Report of a Turkish Child.

Ozcanyuz, Duygu G; Incecik, Faruk; Herguner, Ozlem M; Mungan, Neslihan O; Bozdogan, Sevcan T

Dysarthria, Ataxia, and Dystonia Associated with COX20 (FAM36A) Gene Mutation: A Case Report of a Turkish Child.

Ozcanyuz, Duygu G; Incecik, Faruk; Herguner, Ozlem M; Mungan, Neslihan O; Bozdogan, Sevcan T.

Afiliação

Ozcanyuz DG; Division of Pediatric Neurology, Cukurova University Faculty of Medicine, Adana, Turkey.
Incecik F; Division of Pediatric Neurology, Cukurova University Faculty of Medicine, Adana, Turkey.
Herguner OM; Division of Pediatric Neurology, Cukurova University Faculty of Medicine, Adana, Turkey.
Mungan NO; Division of Pediatric Metabolism, Cukurova University Faculty of Medicine, Adana, Turkey.
Bozdogan ST; Department of Medical Genetics, Cukurova University Faculty of Medicine, Adana, Turkey.

Ann Indian Acad Neurol ; 23(3): 399-401, 2020.

Article em En | MEDLINE | ID: mdl-32606554

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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Revista: Ann Indian Acad Neurol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Turquia

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