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Isolated homozygous R217X OPTN mutation causes knock-out of functional C-terminal optineurin domains and associated oligodendrogliopathy-dominant ALS–TDP
Nolan M., Barbagallo P., Turner MR., Keogh MJ., Chinnery PF., Talbot K., Ansorge O.
DOI
10.1136/jnnp-2020-325803
Type
Journal article
Publisher
BMJ
Publication Date
2021-09-01T00:00:00+00:00
Volume
92
Pages
1022 - 1024
Total pages
2