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Biallelic variants in ZNF142 lead to a syndromic neurodevelopmental disorder. (2022)

First Author: Christensen MB

Attributed to: Leveraging the power of genomics and transcriptomics to revolutionise the diagnosis and understanding of neurological disorders funded by MRC

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