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The phenotypic spectrum associated with loss-of-function variants in monogenic epilepsy genes in the general population. (2023)

First Author: Smuk V

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

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/s41431-022-01211-w

PubMed Identifier: 36253532

Publication URI: http://europepmc.org/abstract/MED/36253532

Type: Journal Article/Review

Volume: 31

Parent Publication: European journal of human genetics : EJHG

Issue: 2

ISSN: 1018-4813