Variants in PRKAR1B cause a neurodevelopmental disorder with autism spectrum disorder, apraxia, and insensitivity to pain. (2021)

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/s41436-021-01152-7

PubMed Identifier: 33833410

Publication URI: http://europepmc.org/abstract/MED/33833410

Type: Journal Article/Review

Volume: 23

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

Issue: 8

ISSN: 1098-3600