Nationwide carrier detection and molecular characterization of β-thalassemia and hemoglobin E variants in Bangladeshi population | Orphanet Journal of Rare Diseases | Full Text

Nationwide carrier detection and molecular characterization of β-thalassemia and hemoglobin E variants in Bangladeshi population | Orphanet Journal of Rare Diseases | Full Text

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

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 ...

Authors:Farjana Akther Noor, Nusrat Sultana, Golam Sarower Bhuyan, Md Tarikul Islam, Mohabbat Hossain, Suprovath Kumar Sarker, Khaleda Islam, Waqar Ahmed Khan, Mujahida Rahman, Syeda Kashfi Qadri, Hossain Uddin Shekhar, Firdausi Qadri, Syed Saleheen Qadri and Kaiissar Mannoor

Citation:Orphanet Journal of Rare Diseases 2020 15:15

Content type:Research

Published on: 15 January 2020

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