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

Hemoglobin - 1 Aug 2002

Krugluger Walter, Hopmeier Pierre

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, Nonsense
Share to DNA Mutational Analysis
Share to Family Health

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

Share to Frameshift Mutation

Share to Globins

Share to Homozygote

Share to Point Mutation

Source

Identifiers

PMID: 12403498
DOI: 10.1081/hem-120015037

Genes

GCA

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 compound beta-thalassemia homozygosity [codon 10 (GCC-->GCA) and codon 16 (-C)] in an Afghan family.PMID 12403498Read ↗

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

Hb I-Toulouse [beta 66(E10)Lys->Glu] in association with alpha-thalassemia.Semantic proximity Read ↗

[Screening and molecular diagnosis for a rare genotype of beta-thalassemia intermedia].Semantic proximity Read ↗

A new beta-thalassemia allele, codon 26 (GAG-->GTAG), found in a Japanese.Semantic proximity Read ↗

Detection of two rare beta-thalassemia alleles found in the Tunisian population: codon 47 (+A) and codons 106/107 (+G).Semantic proximity Read ↗

Hematological and molecular analysis of novel and rare beta-thalassemia mutations in the Indian population.Semantic proximity Read ↗

Rare beta-thalassemia mutation in a Turkish patient: FSC-36/37 (-T).Semantic proximity Read ↗

Beta-thalassemia due to a novel nonsense mutation at codon 37 (TGG-->TAG) found in an Afghanistani family.Semantic proximity Read ↗

Identification of three novel mutations [-41 (A>C), codon 24 (-G), and IVS-I-109 (-T)], in a study of beta-thalassemia alleles in the Isfahan region of Iran.Semantic proximity Read ↗

The β-globin promoter -71 C>T mutation is a β+ thalassemic allele.Semantic proximity Read ↗

Identification of two rare β-globin gene mutations in a patient with β-thalassemia intermedia from Azerbaijan.Semantic proximity Read ↗

A novel beta-thalassemia mutation [codon 45(-T)] in a Pakistani family.Semantic proximity Read ↗

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