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Article

Nondeletional α-thalassemia (α2- IVS-1-116, A>G HBA2): an α2 gene point mutation detected in an African-American female for the first time.

Acta haematologica - 1 Jan 2014

Dainer Paul, Patel Niren, Zhuang Lina, Carmichael Harris, Kutlar Ferdane

Abstract excerpt

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 24356242
DOI: 10.1159/000355426

Genes

HBA2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Nondeletional α-thalassemia (α2- IVS-1-116, A>G HBA2): an α2 gene point mutation detected in an African-American female for the first time.PMID 24356242Read ↗

Nondeletional α-Thalassemia: Two New Mutations on the α2 Gene.Semantic proximity Read ↗

Novel mutations responsible for α-thalassemia in Iranian families.Semantic proximity Read ↗

α(+)-Thalassemia Due to a Frameshift Mutation of the α2-Globin Gene [codons 55/56 (+T) or HBA2: c.168dup].Semantic proximity Read ↗

A novel HBA2 gene conversion in cis or trans: "α12 allele" in a Saudi population.Semantic proximity Read ↗

Interaction of Hb adana (HBA2: c.179G>A) with deletional and nondeletional α(+)-thalassemia mutations: diverse hematological and clinical features.Semantic proximity Read ↗

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

A Rare Alpha-Globin Mutation: Detailed Analysis of the Hb Rogliano Variant (α1 Cod 108 Thr→Asn)Semantic proximity Read ↗

A novel α-thalassemia frameshift mutation: codon 8 (-C).Semantic proximity Read ↗

A Novel α2-Globin Gene Mutation: Hb Debao [α31(B12)Arg→Trp; HBA2: c.94A>T].Semantic proximity Read ↗

Mutations on the α2-Globin Gene That May Trigger α(+)-Thalassemia.Semantic proximity Read ↗

Hb Gerland [alpha55(E4)Val-->Ala (alpha2)]: a new neutral alpha chain variant involving the alpha2 gene.Semantic proximity Read ↗

Two novel α2 gene mutations causing altered amino acid sequences produce a mild (Hb Kinshasa, HBA2: c.428A > T) and severe (HBA2: c.342-345insCC) α-thalassemia phenotype.Semantic proximity Read ↗

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