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

Identification of a novel beta0-thalassemia mutation, codons 80/81 (-C), in an Iranian family.

Hemoglobin - 1 Nov 2000

Feleki X, Najmabadi H, Karimi-Nejad R, Christopoulos G, Kleanthous M

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to beta-Thalassemia
Share to Codon
Share to Globins
Share to Iran

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

Share to Mutation

Source

Identifiers

PMID: 11186262
DOI: 10.3109/03630260008993139

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

Identification of a novel beta0-thalassemia mutation, codons 80/81 (-C), in an Iranian family.PMID 11186262Read ↗

A new beta-thalassemia mutation (initiation codon ATG----GTG) found in the Japanese population.Semantic proximity Read ↗

Rare beta-thalassemia mutations are cause of concern.Semantic proximity Read ↗

Presentation of two new mutations in the 3'untranslated region of the β-globin gene and evaluating the molecular spectrum of thalassemia mutations in the Mediterranean region of Turkey.Semantic proximity Read ↗

A comprehensive molecular characterization of beta thalassemia in a highly heterogeneous population.Semantic proximity Read ↗

A family with the 619 bp deletion on the beta-globin gene found in Kerman Province, Iran.Semantic proximity Read ↗

Characterization of a Novel 71.8 kb α0-Thalassemia Deletion and Subsequent Summary of a Practical Procedure for Thalassemia Molecular Diagnosis.Semantic proximity Read ↗

Identification of a compound beta-thalassemia homozygosity [codon 10 (GCC-->GCA) and codon 16 (-C)] in an Afghan family.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 ↗

Spectrum of beta-thalassemia in Jordan: identification of two novel mutations.Semantic proximity Read ↗

High prevalence of the -alpha3.7 deletion among thalassemia patients in Iran.Semantic proximity Read ↗

Molecular characteristics of α+-thalassemia (3.7 kb deletion) in Southeast Asia: Molecular subtypes, haplotypic heterogeneity, multiple founder effects and laboratory diagnosticsSemantic proximity Read ↗

A novel frameshift mutation: deletion of C in codons 74/75 of the beta-globin gene causes beta zero-thalassemia in a Turkish patient.Semantic proximity Read ↗

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