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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Detalles Bibliográficos
Autores principales: Deo, Sudha S, Bhagat, Ameya R, Shah, Rajnikant N
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications 2011
Materias:
Basic Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3132901/
https://www.ncbi.nlm.nih.gov/pubmed/21772585
http://dx.doi.org/10.4103/0019-5154.82478

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3132901/
https://www.ncbi.nlm.nih.gov/pubmed/21772585
http://dx.doi.org/10.4103/0019-5154.82478

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