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

Novel and unusual deletion-insertion thalassemic mutation in exon 1 of the beta-globin gene.

Human mutation - 1 Jan 1996

Badens C, Thuret I, Michel G, Krawczak M, Mattei J F, Lena-Russo D, Labie D, Elion J

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 Exons
Share to Globins
Share to Haplotypes

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

Share to Infant

Share to Mutagenesis, Insertional

Share to Mutation

Share to Sequence Deletion

Source

Identifiers

PMID: 8807345
DOI: 10.1002/(SICI)1098-1004(1996)8:1<89::AID-HUMU16>3.0.CO;2-N

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

Novel and unusual deletion-insertion thalassemic mutation in exon 1 of the beta-globin gene.PMID 8807345Read ↗

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

Identification of two new alpha-thalassemia mutations in exon 2 of the alpha1-globin gene.Semantic proximity Read ↗

Rare beta-thalassemia mutations are cause of concern.Semantic proximity Read ↗

A rare complex rearrangement in the β-globin gene cluster causing a novel homozygous G γ(A γδβ)0 -thalassemia.Semantic proximity Read ↗

Introduction of novel α1-hemoglobin gene mutation with transfusion-dependent phenotype.Semantic proximity Read ↗

Update in the genetics of thalassemia: What clinicians need to knowSemantic proximity Read ↗

Thalassemia: genotypes and phenotypes.Semantic proximity Read ↗

Two Novel and Five Rare Mutations in the Non Coding Regions of the β-Globin Gene in the Iranian Population.Semantic proximity Read ↗

α-globin gene quadruplication and heterozygous β-thalassemia: a not so rare cause of thalassemia intermedia.Semantic proximity Read ↗

A new beta-thalassemia mutation (initiation codon ATG----GTG) found in the Japanese population.Semantic proximity Read ↗

The beta- and delta-thalassemia repository (7th edition).Semantic proximity Read ↗

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

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