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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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Orphanet J Rare Dis
Prif Awduron: 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
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: BioMed Central 2020
Pynciau:
Research
Mynediad Ar-lein: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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