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A DNA repair disorder caused by de novo monoallelic DDB1 variants is associated with a neurodevelopmental syndrome (2021)

First Author: White S

Attributed to: Developing diagnostic methods for clinical genetics - phenotyping from faces in photos. funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2021.03.007

PubMed Identifier: 33743206

Publication URI: http://europepmc.org/abstract/MED/33743206

Type: Journal Article/Review

Parent Publication: The American Journal of Human Genetics

Issue: 4

ISSN: 0002-9297