Study of variants in genes implicated in rare familial migraine syndromes and their association with migraine in 200,000 exome-sequenced UK Biobank participants. (2022)
Attributed to:
UCL Biosciences Big Data
funded by
BBSRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1111/ahg.12484
PubMed Identifier: 36044383
Publication URI: http://europepmc.org/abstract/MED/36044383
Type: Journal Article/Review
Volume: 86
Parent Publication: Annals of human genetics
Issue: 6
ISSN: 0003-4800