Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Mutation analysis of the HBB gene in selected Bangladeshi beta-thalassemic individuals: presence of rare mutations.

Genetic testing and molecular biomarkers - 1 Jun 2010

Ibn Ayub Mustak, Moosa Mahdi Muhammad, Sarwardi Golam, Khan Waqar, Khan Haseena, Yeasmin Sabina

Abstract excerpt

INTRODUCTION AND AIMS: Bangladesh has a large number of thalassemic patients. However, no extensive analysis of the mutations in the HBB gene of thalassemic patients has been previously carried out. We have conducted a systematic research to reveal thalassemia mutations in the Bangladeshi population. In this preliminary analysis of 587 bp of the HBB gene in selected thalassemic individuals, some rare mutations in...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Asian People
Share to Bangladesh

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to beta-Globins

Share to beta-Thalassemia

Share to DNA Mutational Analysis

Share to Gene Frequency

Share to Genetics, Population

Share to Sequence Analysis, DNA

Source

Identifiers

PMID: 20406103
DOI: 10.1089/gtmb.2009.0160

Genes

HBB

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Mutation analysis of the HBB gene in selected Bangladeshi beta-thalassemic individuals: presence of rare mutations.PMID 20406103Read ↗

The Spectrum of HBB Mutations among 2315 Beta Thalassemia Patients of a Reference Clinic in Tehran-Iran.Semantic proximity Read ↗

Diagnostic Challenges of Borderline A2 Hemoglobin in β-Thalassemia Carriers: Insights from a Bangladeshi CohortSemantic proximity Read ↗

Prenatal Diagnosis and Screening of Thalassemia Mutations in Bangladesh: Presence of Rare Mutations.Semantic proximity Read ↗

The Frequency of HBB Mutations Among β-Thalassemia Patients in Hamadan Province, Iran.Semantic proximity Read ↗

Mutation Spectrum of β-Thalassemia and Other Hemoglobinopathies in Chittagong, Southeast Bangladesh.Semantic proximity Read ↗

Mutational analysis of hemoglobin genes and functional characterization of detected variants, through in-silico analysis, in Pakistani beta-thalassemia major patients.Semantic proximity Read ↗

A comprehensive review of the prevalence of beta globin gene variations and the co-inheritance of related gene variants in Saudi Arabians with beta-thalassemia.Semantic proximity Read ↗

The spectrum of beta-thalassemia mutations in the 22 Arab countries: a systematic review.Semantic proximity Read ↗

α- and β-Globin Gene Mutations in Individuals with Hemoglobinopathies in the Chattogram and Sylhet Regions of Bangladesh.Semantic proximity Read ↗

Rare β-Globin Gene Mutations in Pakistan.Semantic proximity Read ↗

Cross-Sectional Study for the Detection of Mutations in the Beta-Globin Gene Among Patients with Hemoglobinopathies in the Bengali Population.Semantic proximity Read ↗

Spectrum of HBB gene mutations among 696 β-thalassemia patients and carriers in Southern Vietnam.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.