[HTML][HTML] HBB gene mutations and their pathological impacts on HbE/β-Thalassaemia in Kuala Terengganu, Malaysia

HKM Saad, WRW Taib, AS Ab Ghani, I Ismail… - Diagnostics, 2023 - mdpi.com
Background: β-thalassaemia is a disorder caused by mutations in the β-globin gene, leading
to defective production of haemoglobins (Hb) and red blood cells (RBCs). It is characterised …

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

FA Noor, N Sultana, GS Bhuyan, MT Islam… - Orphanet journal of rare …, 2020 - Springer
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 …

[HTML][HTML] Application of targeted next-generation sequencing for the investigation of thalassemia in a developing country: A single center experience

RH Zulkeflee, R Bahar, M Abdullah, MAR Mohd Radzi… - Diagnostics, 2023 - mdpi.com
Thalassemia is identified as a prevalent disease in Malaysia, known to be one of the
developing countries. Fourteen patients with confirmed cases of thalassemia were recruited …

[HTML][HTML] Molecular characterization of α-and β-thalassaemia among Malay patients

NF Mohd Yatim, M Abd. Rahim, K Menon… - International journal of …, 2014 - mdpi.com
Both α-and β-thalassaemia syndromes are public health problems in the multi-ethnic
population of Malaysia. To molecularly characterise the α-and β-thalassaemia deletions and …

[HTML][HTML] Molecular basis of transfusion dependent beta-thalassemia major patients in Sabah

LK Teh, E George, MI Lai, JAMA Tan, L Wong… - Journal of human …, 2014 - nature.com
Beta-thalassemia is one of the most prevalent inherited diseases and a public health
problem in Malaysia. Malaysia is geographically divided into West and East Malaysia. In …

Molecular Characterisation of α‐ and β‐Thalassaemia among Indigenous Senoi Orang Asli Communities in Peninsular Malaysia

DXR Koh, RZA Raja Sabudin… - Annals of human …, 2017 - Wiley Online Library
Thalassaemia is a public health problem in Malaysia, with each ethnic group having their
own common mutations. However, there is a lack on data on the prevalence and common …

Clinical Insights: Prevalence of β-Thalassemia Mutations (IVSI-5, FSC8/9, and CD41/42) in the Swat District

S Saif, S Lila, G Ghani, MA Rahat, A Rasool… - Journal of Bio-X …, 2024 - spj.science.org
Background: Thalassemia is a prevalent condition characterized by decreased production or
absence of hemoglobin globin chains. There are 2 types of thalassemia, alpha thalassemia …

[HTML][HTML] High resolution melting curve analysis targeting the HBB gene mutational hot-spot offers a reliable screening approach for all common as well as most of the …

MT Islam, SK Sarkar, N Sultana, MN Begum… - BMC genetics, 2018 - Springer
Background Bangladesh lies in the global thalassemia belt, which has a defined mutational
hot-spot in the beta-globin gene. The high carrier frequencies of beta-thalassemia trait and …

[HTML][HTML] High throughput molecular confirmation of β-thalassemia mutations using novel TaqMan probes

SL Kho, KH Chua, E George, JAMA Tan - Sensors, 2013 - mdpi.com
β-Thalassemia is a public health problem where 4.5% of Malaysians are β-thalassemia
carriers. The genetic disorder is caused by defects in the β-globin gene complex which lead …

[PDF][PDF] Prevalence of Hb E among adolescents in Basic Education High School, Anisakhan

KM Aung, MM Khaing, NN Thaung… - Journal of Medical and …, 2021 - academia.edu
Haemoglobin (Hb) E is the most common Hb variant found among Southeast Asian
populations. Myanmar also has high prevalence of important haemoglobinopathies: Hb E-1 …