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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Main Authors: Sudha S Deo (Author), Ameya R Bhagat (Author), Rajnikant N Shah (Author)
Format: Book
Published: Wolters Kluwer Medknow Publications, 2011-01-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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