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Repeat expansions in NOP56 are a cause of spinocerebellar ataxia Type 36 in the British population. (2023)

First Author: Lam T

Attributed to: Leveraging the power of genomics and transcriptomics to revolutionise the diagnosis and understanding of neurological disorders funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1093/braincomms/fcad244

PubMed Identifier: 37810464

Publication URI: http://europepmc.org/abstract/MED/37810464

Type: Journal Article/Review

Volume: 5

Parent Publication: Brain communications

Issue: 5

ISSN: 2632-1297