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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Gepubliceerd in:Orphanet J Rare Dis
Hoofdauteurs: 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
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: BioMed Central 2020
Onderwerpen:
Research
Online toegang: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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