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Biallelic POLR3A variants confirmed as a frequent cause of hereditary ataxia and spastic paraparesis

Detalles Bibliográficos
Autores principales:	Rydning, Siri L, Koht, Jeanette, Sheng, Ying, Sowa, Piotr, Hjorthaug, Hanne S, Wedding, Iselin M, Erichsen, Anne Kjersti, Hovden, Inger Anette, Backe, Paul H, Tallaksen, Chantal M E, Vigeland, Magnus D, Selmer, Kaja K
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Oxford University Press 2019
Materias:	Letters to the Editor
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6439323/ https://www.ncbi.nlm.nih.gov/pubmed/30847471 http://dx.doi.org/10.1093/brain/awz041

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