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Missense variants in ANKRD11 cause KBG syndrome by impairment of stability or transcriptional activity of the encoded protein. (2022)

First Author: De Boer E

Attributed to: The Scottish Genomes Partnership funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.gim.2022.06.007

PubMed Identifier: 35833929

Publication URI: http://europepmc.org/abstract/MED/35833929

Type: Journal Article/Review

Volume: 24

Parent Publication: Genetics in medicine : official journal of the American College of Medical Genetics

Issue: 10

ISSN: 1098-3600