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Article

Identification of a novel termination codon mutation (TAA-->TAT, Term-->Tyr) in the alpha 2 globin gene of a Laotian girl with hemoglobin H disease.

Blood - 1 Jun 1994

Waye J S, Eng B, Patterson M, Chui D H, Olivieri N F

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

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Source

Identifiers

PMID: 8193381

Genes

TAT

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 termination codon mutation (TAA-->TAT, Term-->Tyr) in the alpha 2 globin gene of a Laotian girl with hemoglobin H disease.PMID 8193381Read ↗

A novel initiation codon mutation (ATG-->ATT) in a beta-thalassemia patient.Semantic proximity Read ↗

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

Haemoglobin H hydrops fetalis syndrome associated with homozygosity for the alpha2-globin gene polyadenylation signal mutation AATAAA-->AATA- -.Semantic proximity Read ↗

A mutation in the polyadenylation signal of the alpha 2 globin gene (AATAAA-->AATA--) as a cause of alpha thalassaemia in Asian indians.Semantic proximity Read ↗

A novel polyadenylation signal mutation in the α<sub>2</sub>‐globin gene causing α thalassaemiaSemantic proximity Read ↗

Compound heterozygosity for two alpha-globin gene defects, Hb Taybe (alpha 1; 38 or 39 minus Thr) and a poly A mutation (alpha 2; AATAAA-->AATAAG), results in a severe hemolytic anemia.Semantic proximity Read ↗

Initiation codon mutation (ATG --> ATA) of the beta-globin gene causing beta-thalassemia in a Swedish family.Semantic proximity Read ↗

Identification of a novel A allele with initiator codon variant (c.2T > A) in the ABO gene associated with weak A phenotype.Semantic proximity Read ↗

Tertiary structural analysis of the elongated part of an abnormal hemoglobin, hemoglobin Pakse.Semantic proximity Read ↗

Molecular and cellular analysis of a novel HBA2 mutation (HBA2: c.94A > G) shows activation of a cryptic splice site and generation of a premature termination codon.Semantic proximity Read ↗

Identification of several alpha-globin gene variations in a small Laotian family.Semantic proximity Read ↗

Complete thyroxine-binding globulin (TBG) deficiency produced by a mutation in acceptor splice site causing frameshift and early termination of translation (TBG-Kankakee).Semantic proximity Read ↗

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