Nationwide carrier detection and molecular characterization of β-thalassemia and hemoglobin E variants in Bangladeshi population

BACKGROUND: ß-thalassemia is one of the most common inherited blood disorders in the world and a major deterrent to the public health of Bangladesh. The management of thalassemia patients requires lifelong frequent blood transfusion and the available treatment options are unsatisfactory. A national...

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Detalles Bibliográficos
Autores principales: Noor, Farjana Akther, Sultana, Nusrat, Bhuyan, Golam Sarower, Islam, Md Tarikul, Hossain, Mohabbat, Sarker, Suprovath Kumar, Islam, Khaleda, Khan, Waqar Ahmed, Rahman, Mujahida, Qadri, Syeda Kashfi, Shekhar, Hossain Uddin, Qadri, Firdausi, Qadri, Syed Saleheen, Mannoor, Kaiissar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6961315/
https://www.ncbi.nlm.nih.gov/pubmed/31941534
http://dx.doi.org/10.1186/s13023-020-1294-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6961315/
https://www.ncbi.nlm.nih.gov/pubmed/31941534
http://dx.doi.org/10.1186/s13023-020-1294-z

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