Literature DB >> 1148221

Hemoglobin-A2-Coburg or alpha2delta2116Arg leads to His (G18).

R S Sharma, L Williams, J B Wilson, T H Huisman.   

Abstract

Hemoglobin-A2-Coburg or alpha2delta2-116 Arg leads to His (G18) has been found in members of a family of Sicilian origin. The propositus is heterozygous for hemoglobin-A2-Coburg as well as for beta-thalassemia, and family data indicate that the gene for the delta-Coburg chain is in trans of the beta-thalassemia determinant.

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Year:  1975        PMID： 1148221     DOI： 10.1016/0005-2795(75)90065-3

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN： 0006-3002


  3 in total

1.  A new delta chain variant hemoglobin A2-Corfu or alpha 2 delta 2 116 Arg----Cys (G18), detected by delta-globin gene analysis in a Greek family.

Authors:  G Loudianos; S Murru; E Kanavakis; A Metaxotou-Mavromati; D Theodoropoulou; C Kattamis; A Cao; M Pirastu
Journal:  Hum Genet       Date:  1991-06       Impact factor: 4.132

2.  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

3.  Evidence that structural variants within the human delta-globin protein may reflect genetic interactions between the delta- and beta-globin genes.

Authors:  T D Petes
Journal:  Am J Hum Genet       Date:  1982-09       Impact factor: 11.025
  3 in total

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