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A Distinct Genotype of XP Complementation Group A: Surprisingly Mild Phenotype Highly Prevalent in Northern India/Pakistan/Afghanistan. (2016)

First Author: Sethi M

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/10.1016/j.jid.2015.12.031

PubMed Identifier: 26743599

Publication URI: http://europepmc.org/abstract/MED/26743599

Type: Journal Article/Review

Volume: 136

Parent Publication: The Journal of investigative dermatology

Issue: 4

ISSN: 0022-202X