Biallelic variants in ZNF142 lead to a syndromic neurodevelopmental disorder. (2022)
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1111/cge.14165
PubMed Identifier: 35616059
Publication URI: http://europepmc.org/abstract/MED/35616059
Type: Journal Article/Review
Volume: 102
Parent Publication: Clinical genetics
Issue: 2
ISSN: 0009-9163