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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)

First Author: Markel KA

Attributed to: UK Biobank (core renewal) funded by MRC

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