📣 Try out the NEW Gateway to Research and let us know what you think.

We're looking for users to test the new service during August and September and share their feedback. Express your interest by completing this short form.

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