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

Beta 0-thalassemia due to a cytosine deletion in codon 41 associated with hemoglobin E.

The Southeast Asian journal of tropical medicine and public health - 1 Jun 1993

Petmitr S, Fucharoen S, Rajkulchai P, Bifani J P, Wilairat P

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 Base Sequence
Share to beta-Thalassemia
Share to Codon
Share to Gene Deletion

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

Share to Hemoglobin E

Share to Molecular Sequence Data

Share to Mutation

Share to Thailand

Source

Identifiers

PMID: 8266246

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

Beta 0-thalassemia due to a cytosine deletion in codon 41 associated with hemoglobin E.PMID 8266246Read ↗

Thalassemia major phenotypes secondary to the association of β 5'UTR +20(C → T) allele with β 39(C → T).Semantic proximity Read ↗

b-thalassemia intermedia resulting from compound heterozigosity for an IVSI-1 (G-A) and a silent 5' UTR +33 (C-G) mutations.Semantic proximity Read ↗

Hb G-Honolulu [alpha30(B11)Glu-->Gln (alpha2)], Hb J-Meinung [beta56(D7)Gly-->Asp], and beta-thalassemia [codons 41/42 (-TCTT)] in a Taiwanese family.Semantic proximity Read ↗

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

Compound heterozygote condition in beta thalassemia major due to a novel single nucleotide deletion (-T) at codon 69 in association with IVS 1-5 (G>C) mutation.Semantic proximity Read ↗

A novel beta-thalassemia mutation (G-->A) at the initiation codon of the beta-globin gene.Semantic proximity Read ↗

Historical note: the beta-thalassemia allele in the noble Russian family Lermontov is identified as the ATG-->ACG change in the initiation codon.Semantic proximity Read ↗

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

Mild Hb S-beta(+)-thalassemia with a deletion of five nucleotides at the polyadenylation site of the beta-globin gene.Semantic proximity Read ↗

Novel beta 0-thalassemia mutation in a Canadian woman of British descent (codons 72/73, -AGTGA, +T).Semantic proximity Read ↗

Two novel beta-thalassemia alleles: poly A signal (AATAAA-->AAAA) and -92 C-->T.Semantic proximity Read ↗

Nonsense mutation of β-globin gene at codon 82 (AAG→TAG) or HBB:C247 A→T with polymorphism: cause of thalassemia intermedia?Semantic proximity Read ↗

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