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

Internet

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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