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

Internet

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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