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Association of ultra-rare coding variants with genetic generalized epilepsy: A case-control whole exome sequencing study. (2022)

First Author: Koko M

Attributed to: HSM:Development of methodology and computationally efficient software for analysis of PGx exome sequencing studies of complex "time-to-event" outcomes funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1111/epi.17166

PubMed Identifier: 35032048

Publication URI: http://europepmc.org/abstract/MED/35032048

Type: Journal Article/Review

Volume: 63

Parent Publication: Epilepsia

Issue: 3

ISSN: 0013-9580