Novel PNKP mutations associated with reduced DNA single-strand break repair and severe microcephaly, seizures, and developmental delay. (2024)
Attributed to:
Mechanisms of DNA Single-Strand Break-Induced Genetic Disease and Opportunities for Therapeutic Intervention
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1002/mgg3.2295
PubMed Identifier: 37916443
Publication URI: http://europepmc.org/abstract/MED/37916443
Type: Journal Article/Review
Volume: 12
Parent Publication: Molecular genetics & genomic medicine
Issue: 1
ISSN: 2324-9269