Detection of Common Deletional of α-Thalassemia 3.7 Kb from Metropolitan Region of Manaus, Amazonas, Brazil

BACKGROUND: Alpha Thalassemia (α-thal) is a heterogeneous group of hereditary alterations caused by deletions that affect alpha regulatory genes, and the 3.7Kb deletion is the most frequent worldwide. The prevalence ranges from 20% and 35% in Brazil, depending mainly on race, predominant in Afro-des...

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Detalles Bibliográficos
Autores principales: Anselmo, Fernanda Cozendey, Soumanou, Abdou Gafar, de Aguiar Ferreira, Cleidiane, Sobrinha, Flora Maia Viga, Castro, Ana Caroline Santos, Brito, Rafael Oliveira, da Mota, Adolfo José, de Souza Gonçalves, Marilda, de Moura Neto, José Pereira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Università Cattolica del Sacro Cuore 2021
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7813276/
https://www.ncbi.nlm.nih.gov/pubmed/33489040
http://dx.doi.org/10.4084/MJHID.2021.001

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7813276/
https://www.ncbi.nlm.nih.gov/pubmed/33489040
http://dx.doi.org/10.4084/MJHID.2021.001

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