Literature DB >> 14081243

HEMOGLOBIN G-COUSHATTA: A NEW VARIANT IN AN AMERICAN INDIAN FAMILY.

R G SCHNEIDER, M E HAGGARD, C W MCNUTT, J E JOHNSON.   

Abstract

A new hemoglobin variant, G(couhatta) (alpha2(A) beta2(iiiglu-->ala)), has been found in three generations of a family from the Alabama Coushatta Indian tribe in east Texas. The propositus suffers from an apparently unrelated, possibly genetic, agranulocytosis. According to the history and the blood grouping data there is considerable in breeding in the tribe and remarkably little admixture with other ethnic groups.

Entities:  

Keywords:  AGRANULOCYTOSIS; HEMOGLOBINS, ABNORMAL; INDIANS, NORTH AMERICAN

Mesh:

Substances:

Year:  1964        PMID: 14081243     DOI: 10.1126/science.143.3607.697

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  5 in total

1.  Partial mispairing and crossing-over between beta 0 and delta genes as the origin of the delta beta 0 thalassemia gene. A single mutational event hypothesis.

Authors:  J M Cantú; B Ibarra; G Vaca; M L Ramirez; J Sánchez-Corona
Journal:  Hum Genet       Date:  1979-06-19       Impact factor: 4.132

Review 2.  Haemoglobin D Punjab (D Los Angeles).

Authors:  F Vella; H Lehmann
Journal:  J Med Genet       Date:  1974-12       Impact factor: 6.318

3.  High incidence of haemoglobin G Accra in a rural district in Jamaica.

Authors:  P F Milner
Journal:  J Med Genet       Date:  1967-06       Impact factor: 6.318

4.  Study on hemoglobinopathies in Hubei Province: report of hemoglobin GCoushatta homozygotes and hemoglobin GTaibei heterozygotes.

Authors:  B Y Wang; Y C Gu; Y Q Luo; A Yang; Y T Zeng; S Z Huang
Journal:  Acta Acad Med Wuhan       Date:  1982

5.  Estimating the age of Hb G-Coushatta [β22(B4)Glu→Ala] mutation by haplotypes of β-globin gene cluster in Denizli, Turkey.

Authors:  Onur Ozturk; Sanem Arikan; Ayfer Atalay; Erol O Atalay
Journal:  Mol Genet Genomic Med       Date:  2018-05-01       Impact factor: 2.183

  5 in total

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