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Article

Hb Manitoba in a Taiwanese family: a C-->A substitution at codon 102 of the alpha2-globin gene.

Hemoglobin - 1 Nov 2001

Chang J G, Shih M C, Liu S C, Chan W L, Peng C T

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Identifiers

PMID: 11791879
DOI: 10.1081/hem-100107883

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Hb Manitoba in a Taiwanese family: a C-->A substitution at codon 102 of the alpha2-globin gene.PMID 11791879Read ↗

Hb Manitoba [α102(G9)Ser→Arg] in Pasifika: Tongan Case Report.Semantic proximity Read ↗

Hb G-Honolulu [alpha30(B11)Glu-->Gln (alpha2)], Hb J-Meinung [beta56(D7)Gly-->Asp], and beta-thalassemia [codons 41/42 (-TCTT)] in a Taiwanese family.Semantic proximity Read ↗

Mutations in the paralogous human alpha-globin genes yielding identical hemoglobin variants.Semantic proximity Read ↗

Twelve Cases of Hb Manitoba [α102(G9)Ser→Arg]: the Fluctuation in the Variant Expression.Semantic proximity Read ↗

The first case of Hb E-Saskatoon [alpha 2 beta(2)22(B4)Glu-->Lys] in a Japanese male in Asia.Semantic proximity Read ↗

Four new variants of the alpha2-globin gene without clinical or hematologic effects: Hb Park Ridge [alpha9(alpha7)Asn-->Lys (alpha2)], Hb Norton [alpha72(EF1)His-->Asp (alpha2)], Hb Lombard [alpha103(G10)His-->Tyr (alpha2)], and Hb San Antonio [A113(GH2)Leu-->Arg (A2)].Semantic proximity Read ↗

Hb Manawatu [alpha 37(C2)Pro-->Leu]: a new mildly unstable mutation at an invariant proline residue.Semantic proximity Read ↗

A novel beta-globin mutation (HBB:c.107A>G; or codon 35 beta (A-->G)) at alpha-beta chain interfaces.Semantic proximity Read ↗

Hb Porto Alegre or alpha 2 beta 29(A6)Ser->Cys in unrelated families of the Canary Islands.Semantic proximity Read ↗

Novel beta 0-thalassemia mutation in a Canadian woman of British descent (codons 72/73, -AGTGA, +T).Semantic proximity Read ↗

First Report of Nondeletional Hb H Disease Caused by an α2-Globin Gene Mutation: HBA2: c.184A>T.Semantic proximity Read ↗

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.Semantic proximity Read ↗

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