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Articles Related to CPD

Xeroderma Pigmentosum Groups C and A in Algerian Patients with Deregulation of both Transcription and DNA Repair

Xeroderma Pigmentosum (XP) is a rare autosomal recessive disorder characterized by an extreme sensitivity to UV rays from sunlight, a high incidence of skin cancer and occasional neurological symptoms. XP, primarily defined as a DNA repair syndrome, has been found associated with defects in the Nucleotide Excision Repair (NER) pathway, and more recently by transcriptional deregulation. XP results from mutations in eight genes (XPA to XPG and XPV) coding for proteins involved in NER.
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Editorial Board Members Related to CPD

Mohamed Abdo Rizk

Professor
Department of Internal Medicine and Infectious Diseases
Mansoura University
Egypt

Michael Zhuo Wang

Assistant Professor
Department of Pharmaceutical Chemistry
The University of Kansas
United States
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