Isolated homozygous R217X OPTN mutation causes knock-out of functional C-terminal optineurin domains and associated oligodendrogliopathy-dominant ALS–TDP

Detalles Bibliográficos
Autores principales: Nolan, Matthew, Barbagallo, Paola, Turner, Martin R, Keogh, Michael John, Chinnery, Patrick F, Talbot, Kevin, Ansorge, Olaf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2021
Materias:
PostScript
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8372379/
https://www.ncbi.nlm.nih.gov/pubmed/33727253
http://dx.doi.org/10.1136/jnnp-2020-325803

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8372379/
https://www.ncbi.nlm.nih.gov/pubmed/33727253
http://dx.doi.org/10.1136/jnnp-2020-325803

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