Whole genome sequencing for the diagnosis of neurological repeat expansion disorders in the UK: a retrospective diagnostic accuracy and prospective clinical validation study (2022)
Abstract
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Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1016/s1474-4422(21)00462-2
PubMed Identifier: 35182509
Publication URI: http://europepmc.org/abstract/MED/35182509
Type: Journal Article/Review
Parent Publication: The Lancet Neurology
Issue: 3
ISSN: 1474-4422