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

The first report of a homozygous codons 9/10 (+T) β-thalassemia mutation in a Turkish patient.

Hemoglobin - 1 Jan 2015

Unal Sule, Chui David H K, Luo Hong-Yuan, Okur Hamza, Oymak Yesim, Gumruk Fatma

Abstract excerpt

For the first time in Turkey, we report a thalassemic patient with a homozygous codons 9/10 (+T) genotype. Currently, the patient is 3 years and 2 months old and received an initial transfusion at the age of 18 months. After being alloimmunized following this transfusion, he required frequent transfusions, every week to every other week. Although alloimmunization was controlled after methyl-prednisolone,...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to beta-Globins
Share to beta-Thalassemia
Share to Blood Transfusion

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Homozygote

Share to Pregnancy

Share to Splenectomy

Share to Turkey

Source

Identifiers

PMID: 25572182
DOI: 10.3109/03630269.2014.982255

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 11 closest

The first report of a homozygous codons 9/10 (+T) β-thalassemia mutation in a Turkish patient.PMID 25572182Read ↗

The carrier frequency of α-globin gene triplication in an Iranian population with normal or borderline hematological parameters.Semantic proximity Read ↗

The codons 8/9 (+G) mutation found for the first time in the Lebanese population.Semantic proximity Read ↗

"Silent" β-thalassemia mutation (promoter nt-101 C > T) with increased hemoglobin A2.Semantic proximity Read ↗

Identification of a compound beta-thalassemia homozygosity [codon 10 (GCC-->GCA) and codon 16 (-C)] in an Afghan family.Semantic proximity Read ↗

β-Globin Gene Mutations in Pediatric Patients with β-Thalassemia in the Region of Çukurova, Turkey.Semantic proximity Read ↗

Identification of a new mutation on the beta-globin gene: codons 8/9 (+AGAA); GAG.AAG.TCT(Glu-Lys-Ser)>GAG. AAAGAAG, in a patient from the north of France with a phenotype of beta-thalassemia minor.Semantic proximity Read ↗

Rare Pathogenic β0-Thalassemia Mutation, Codon 7 (GAG>TAG) (HBB: c.22G>T). Report of the First Two Cases in Albanian Immigrants of Northern Greece.Semantic proximity Read ↗

A novel frameshift mutation: deletion of C in codons 74/75 of the beta-globin gene causes beta zero-thalassemia in a Turkish patient.Semantic proximity Read ↗

Detection of a Rare Mutation in the Initiation Codon of the β-Globin Gene (HBB:C.2T > C; P.Met1Thr).Semantic proximity Read ↗

A frameshift at codons 77/78 (-C): a novel beta-thalassemia mutation.Semantic proximity Read ↗

Rare beta-thalassemia mutation in a Turkish patient: FSC-36/37 (-T).Semantic proximity Read ↗

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