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Deep phenotyping of 89 xeroderma pigmentosum patients reveals unexpected heterogeneity dependent on the precise molecular defect. (2016)

First Author: Fassihi H

Attributed to: Xeroderma pigmentosum: a model to study molecular, cellular and clinical consequences of specific defects in the nucleotide excision repair pathway funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1073/pnas.1519444113

PubMed Identifier: 26884178

Publication URI: http://europepmc.org/abstract/MED/26884178

Type: Journal Article/Review

Volume: 113

Parent Publication: Proceedings of the National Academy of Sciences of the United States of America

Issue: 9

ISSN: 0027-8424