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Comprehensive EHMT1 variants analysis broadens genotype-phenotype associations and molecular mechanisms in Kleefstra syndrome. (2024)

First Author: Rots D

Attributed to: ICF: Epigenomics Rare Diseases Node funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2024.06.008

PubMed Identifier: 39013458

Publication URI: http://europepmc.org/abstract/MED/39013458

Type: Journal Article/Review

Volume: 111

Parent Publication: American journal of human genetics

Issue: 8

ISSN: 0002-9297