Pellagra-like condition is xeroderma pigmentosum/Cockayne syndrome complex and niacin confers clinical benefit

Xeroderma pigmentosum complementation group G patient with a novel homozygous missense mutation and no neurological abnormalities

(2012) Shinichi Moriwaki et al.   EXPERIMENTAL DERMATOLOGY

NovelXPG(ERCC5) Mutations AffectDNARepair and Cell Survival after Ultraviolet but not Oxidative Stress

(2012) Daniela T. Soltys et al.   HUMAN MUTATION

Effects of Niacin Restriction on Sirtuin and PARP Responses to Photodamage in Human Skin

(2012) Claudia A. Benavente et al.   PLoS One

Neuroimaging In Cockayne Syndrome

(2010) M. Koob et al.   AMERICAN JOURNAL OF NEURORADIOLOGY

Pellagra: a review with emphasis on photosensitivity

(2010) P. Wan et al.   BRITISH JOURNAL OF DERMATOLOGY

Disorders of nucleotide excision repair: the genetic and molecular basis of heterogeneity

(2009) James E. Cleaver et al.   NATURE REVIEWS GENETICS