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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Detalhes bibliográficos
Publicado no:Orphanet J Rare Dis
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2020
Assuntos:
Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6961315/
https://ncbi.nlm.nih.gov/pubmed/31941534
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-020-1294-z
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