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Clustered variants in the 5' coding region of TRA2B cause a distinctive neurodevelopmental syndrome. (2023)

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.gim.2022.100003

PubMed Identifier: 36549593

Publication URI: http://europepmc.org/abstract/MED/36549593

Type: Journal Article/Review

Volume: 25

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

Issue: 4

ISSN: 1098-3600