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Novel PNKP mutations causing defective DNA strand break repair and PARP1 hyperactivity in MCSZ. (2019)

First Author: Kalasova I

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1212/nxg.0000000000000320

PubMed Identifier: 31041400

Publication URI: http://europepmc.org/abstract/MED/31041400

Type: Journal Article/Review

Volume: 5

Parent Publication: Neurology. Genetics

Issue: 2

ISSN: 2376-7839