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Inactivating TDP2 missense mutation in siblings with congenital abnormalities reminiscent of fanconi anemia. (2023)

First Author: Zagnoli-Vieira G

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