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

Spectrum of β-thalassemia mutations in the eastern province of Saudi Arabia.

Hemoglobin - 1 Jan 2011

Al-Sultan Ali, Phanasgaonkar Supriya, Suliman Ahmed, Al-Baqushi Muneer, Nasrullah Zaki, Al-Ali Amein

Abstract excerpt

β-Thalassemias comprise a group of heterogeneous hemoglobin (Hb) disorders characterized by the absence or reduced synthesis of the β-globin chain with a variable clinical presentation. The Al-Qatif and Al-Ahsa oases in the Eastern Province of Saudi Arabia are regions known for the high prevalence of these disorders. This study was conducted to provide a more precise picture of the β-thalassemia (β-thal)...

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to Alleles
Share to beta-Thalassemia

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Child, Preschool

Share to Gene Frequency

Share to Genotype

Share to Mutation

Source

Identifiers

PMID: 21417569
DOI: 10.3109/03630269.2011.553567

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Spectrum of β-thalassemia mutations in the eastern province of Saudi Arabia.PMID 21417569Read ↗

Spectrum of α-thalassemia mutations in transfusion-dependent β-thalassemia patients from the Eastern Province of Saudi Arabia.Semantic proximity Read ↗

Mutation Spectrum of Hemoglobinopathies in Tunisia.Semantic proximity Read ↗

β-Globin Mutations in Egyptian Patients With β-Thalassemia.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 ↗

Rare hemoglobin variants in Tunisian population.Semantic proximity Read ↗

The Spectrum of β-Thalassemia Mutations in the Population Migration in Lebanon: A 6-Year Retrospective Study.Semantic proximity Read ↗

Molecular spectrum of α-thalassemia mutations in Erbil province of Iraqi Kurdistan.Semantic proximity Read ↗

Molecular Basis of β-Thalassemia in the Population of the Aegean Region of Turkey: Identification of A Novel Deletion Mutation.Semantic proximity Read ↗

Molecular basis of β-thalassemia in the western province of Saudi Arabia: identification of rare β-thalassemia mutations.Semantic proximity Read ↗

α-Globin Genotypes Associated with Hb H Disease: A Report from Oman and a Review of the Literature from the Eastern Mediterranean Region.Semantic proximity Read ↗

Prevalence and Regional Distribution of Beta-Hemoglobin Variants in Saudi Arabia: Insights from the National Premarital Screening Program" Running Title: Burden of Beta-Globin Variants in Saudi ArabiaSemantic proximity Read ↗

Analysis of δ-globin gene alleles in Tunisians: description of three new delta-thalassemia mutations.Semantic proximity Read ↗

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