CFI-rs7356506 polymorphisms associated with Vogt-Koyanagi-Harada syndrome

PURPOSE: Complement factor I (CFI) plays an important role in complement activation pathways and is known to affect the development of uveitis. The present study was performed to investigate the existence of an association between CFI genetic polymorphisms and Vogt-Koyanagi-Harada (VKH) syndrome. ME...

Descripción completa

Detalles Bibliográficos
Autores principales: Dai, Ma-Li, Huang, Xiu-Feng, Wang, Qing-Feng, Cai, Wei-Jun, Jin, Zi-Bing, Wang, Yuqin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4734154/
https://www.ncbi.nlm.nih.gov/pubmed/26900322

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4734154/
https://www.ncbi.nlm.nih.gov/pubmed/26900322

Ejemplares similares