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Article

A novel mutation (nonsense beta 127) in exon 3 of the beta globin gene produces a variable thalassaemic phenotype.

British journal of haematology - 1 Oct 1991

Hall G W, Franklin I M, Sura T, Thein S L

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Source

Identifiers

PMID: 1958498
DOI: 10.1111/j.1365-2141.1991.tb04548.x

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

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

A novel mutation (nonsense beta 127) in exon 3 of the beta globin gene produces a variable thalassaemic phenotype.PMID 1958498Read ↗

Dominant thalassemia-like phenotypes associated with mutations in exon 3 of the beta-globin gene.Semantic proximity Read ↗

A single nucleotide deletion in codon 123 of the beta-globin gene causes an inclusion body beta-thalassaemia trait: a novel elongated globin chain beta Makabe.Semantic proximity Read ↗

The -87 (C----A) beta(+)-thalassemia mutation in a black family.Semantic proximity Read ↗

A new alpha2-globin gene [codon 90 (AAG --> TAG)] nonsense mutation.Semantic proximity Read ↗

Three new beta-thalassemia mutations with varying degrees of severity.Semantic proximity Read ↗

A mutation of CDS 82/83 (-G) observed in a Yugoslavian family with a heterozygosity for beta-thalassemia.Semantic proximity Read ↗

Eight-base deletion in exon 3 of the beta-globin gene produced a novel variant (beta khon kaen) with an inclusion body beta-thalassemia trait.Semantic proximity Read ↗

A deletion of 11 bp (CD 131-134) in exon 3 of the beta-globin gene produces the phenotype of inclusion body beta-thalassemia.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 new alpha alpha alpha anti-3.7 alpha-globin allele.Semantic proximity Read ↗

Type I Glanzmann thrombasthenia caused by an apparently silent beta3 mutation that results in aberrant splicing and reduced beta3 mRNA.Semantic proximity Read ↗

Hb Lynwood [α107(G14) (-T) (α2) HBA2:c.323delT)] in conjunction with the α(3.7) deletion produces a moderately severe α-thalassemia phenotype.Semantic proximity Read ↗

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