Investigation of mutations in the HBB gene using the 1,000 genomes database.

Investigation of mutations in the HBB gene using the 1,000 genomes database.

Mutations in the HBB gene are responsible for several serious hemoglobinopathies, such as sickle cell anemia and β-thalassemia. Sickle cell anemia is one of the most common monogenic diseases worldwide. Due to its prevalence, diverse strategies have been developed for a better understanding of its m...

Full description

Bibliographic Details
Main Authors: Tânia Carlice-Dos-Reis, Jaime Viana, Fabiano Cordeiro Moreira, Greice de Lemos Cardoso, João Guerreiro, Sidney Santos, Ândrea Ribeiro-Dos-Santos
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5381778?pdf=render

Internet

http://europepmc.org/articles/PMC5381778?pdf=render

Similar Items