Lack of Association between PTPN22 Gene +1858 C>T Polymorphism and Susceptibility to Generalized Vitiligo in a Turkish Population

BACKGROUND: Vitiligo is an autoimmune polygenic disorder characterized by loss of pigmentation due to melanocyte destruction. The PTPN22 gene +1858 C>T single nucleotide polymorphism (rs2476601) has been shown to be associated with various autoimmune disorders. OBJECTIVE: The aim of this study wa...

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Detalles Bibliográficos
Autores principales: Akbas, Halit, Dertlioglu, Selma Bakar, Dilmec, Fuat, Atay, Ahmet Engin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Dermatological Association; The Korean Society for Investigative Dermatology 2014
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3956800/
https://www.ncbi.nlm.nih.gov/pubmed/24648691
http://dx.doi.org/10.5021/ad.2014.26.1.88

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3956800/
https://www.ncbi.nlm.nih.gov/pubmed/24648691
http://dx.doi.org/10.5021/ad.2014.26.1.88

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