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...

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Detalles Bibliográficos
Autores principales: Carlice-dos-Reis, Tânia, Viana, Jaime, Moreira, Fabiano Cordeiro, Cardoso, Greice de Lemos, Guerreiro, João, Santos, Sidney, Ribeiro-dos-Santos, Ândrea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5381778/
https://www.ncbi.nlm.nih.gov/pubmed/28379995
http://dx.doi.org/10.1371/journal.pone.0174637

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5381778/
https://www.ncbi.nlm.nih.gov/pubmed/28379995
http://dx.doi.org/10.1371/journal.pone.0174637

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