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Compound heterozygous loss-of-function mutations in KIF20A are associated with a novel lethal congenital cardiomyopathy in two siblings. (2018)

First Author: Louw JJ

Attributed to: Systems-level characterization of mammalian cell cycle transitions funded by BBSRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1371/journal.pgen.1007138

PubMed Identifier: 29357359

Publication URI: http://europepmc.org/abstract/MED/29357359

Type: Journal Article/Review

Volume: 14

Parent Publication: PLoS genetics

Issue: 1

ISSN: 1553-7390