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

Homozygous non-deletion alpha 2 globin gene mutation (initiation codon mutation): clinical and haematological phenotype.

British journal of haematology - 1 Sept 1991

Galanello R, Monne M I, Paderi L, Paglietti E, Atzori G, Addis M, Limongelli O, Macciotta A, Cao A

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 Child
Share to Child, Preschool
Share to Codon
Share to Globins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Infant

Share to Mutation

Share to Phenotype

Share to Thalassemia

Source

Identifiers

PMID: 1911369
DOI: 10.1111/j.1365-2141.1991.tb08018.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

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Homozygous non-deletion alpha 2 globin gene mutation (initiation codon mutation): clinical and haematological phenotype.PMID 1911369Read ↗

The alpha-globin gene cluster: genetics and disorders.Semantic proximity Read ↗

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

Fibrinogen storage disease caused by Aguadilla mutation presenting with hypobeta-lipoproteinemia and considerable liver disease.Semantic proximity Read ↗

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

Hematological phenotype of carriers of deletion alpha-thalassemia according to the alpha-globin genotype.Semantic proximity Read ↗

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

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

SERAC1 gene mutation presented with markedly alpha fetoprotein elevation: case report.Semantic proximity Read ↗

Molecular and Hematological Characterization of a Novel Translation Initiation Codon Mutation of the α2-Globin Gene (ATG>ATC or HBA2: c.3G>C).Semantic proximity Read ↗

An alpha-thalassemic hemoglobinopathy: homozygosity for the HB Agrinio alpha 2-globin chain variant.Semantic proximity Read ↗

An insight of -50 (G>A) mutation in the direct repeat element of the β-globin gene: From Malaysian perspective.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.