Inactivating TDP2 missense mutation in siblings with congenital abnormalities reminiscent of fanconi anemia. (2023)
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/10.1007/s00439-023-02589-3
PubMed Identifier: 37558815
Publication URI: http://europepmc.org/abstract/MED/37558815
Type: Journal Article/Review
Volume: 142
Parent Publication: Human genetics
Issue: 9
ISSN: 0340-6717