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

Detalles Bibliográficos
Autores principales:	Ozcanyuz, Duygu G., Incecik, Faruk, Herguner, Ozlem M., Mungan, Neslihan O., Bozdogan, Sevcan T.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Wolters Kluwer - Medknow 2020
Materias:	Letters to the Editor
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7313588/ https://www.ncbi.nlm.nih.gov/pubmed/32606554 http://dx.doi.org/10.4103/aian.AIAN_536_19

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