Genetic variations in NALP1 MRNA expressions in human vitiligo

Introduction: Vitiligo is an acquired autoimmune disease of unknown etiology showing depigmentation of the skin due to the absence of melanocytes. Familial vitiligo suggests a genetic origin to this disease. Chromosome 17 was recently demonstrated to harbor the gene coding for NALP1. Patients and Me...

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Bibliographic Details
Main Authors: Sudha S Deo, Ameya R Bhagat, Rajnikant N Shah
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2011-01-01
Series:Indian Journal of Dermatology
Subjects:
Online Access:http://www.e-ijd.org/article.asp?issn=0019-5154;year=2011;volume=56;issue=3;spage=266;epage=271;aulast=Deo