IL10 Low-Frequency Variants in Behçet's Disease Patients

To explain the missing heritability after the genome-wide association studies era, sequencing studies allow the identification of low-frequency variants with a stronger effect on disease risk. Common variants in the interleukin 10 gene (IL10) have been consistently associated with Behçet's dise...

Full description

Bibliographic Details
Main Author: Matos, M (author)
Other Authors: Xavier, JM (author), Abrantes, P (author), Sousa, I (author), Rei, N (author), Davatchi, F (author), Shahram, F (author), Jesus, G (author), Barcelos, F (author), Vedes, J (author), Salgado, Manuel (author), Abdollahi, B (author), Nadji, A (author), Moraes-Fontes, MF (author), Shafiee, N (author), Ghaderibarmi, F (author), Vaz Patto, J (author), Crespo, J (author), Oliveira, SA (author)
Format: article
Language:eng
Published: 2016
Subjects:
Behçet's disease
IL10
Low-frequency variants
HCC DAUTOIM
Online Access:http://hdl.handle.net/10400.17/2548
Country:Portugal
Oai:oai:repositorio.chlc.min-saude.pt:10400.17/2548

Internet

http://hdl.handle.net/10400.17/2548

Similar Items