Literature DB >> 3804326

Population structure of Sicily: beta-thalassemia and HbS.

I Barrai, G Schiliro, M Beretta, P Mazzetti, A Russo, G Russo Mancuso.   

Abstract

The population structure of two alleles with similar characteristics, HbS and beta-thalassemia, was studied in the same area in Sicily. It was observed that beta-thalassemia has uniform frequencies over the island, and that HbS shows a South-North cline. A singularity exists for HbS in the town of Butera, where the frequency of the S gene is six times higher than the island average. It was suggested that HbS entered Sicily from Greece (or directly from North Africa) when the beta-thalassemia allele was already established in the Island.

Entities:  

Mesh:

Year:  1987        PMID: 3804326     DOI: 10.1007/bf00273828

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  7 in total

1.  STUDIES ON THE DISTRIBUTION OF GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY, THALASSEMIA, AND OTHER GENETIC TRAITS IN THE COASTAL AND MOUNTAIN VILLAGES OF CYPRUS.

Authors:  C C PLATO; D L RUCKNAGEL; H GERSHOWITZ
Journal:  Am J Hum Genet       Date:  1964-09       Impact factor: 11.025

2.  Aspects of polymorphism in man.

Authors:  A C ALLISON
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1955

3.  Population structure and historical genetics of isolates.

Authors:  N E Morton
Journal:  Isr J Med Sci       Date:  1973 Sep-Oct

4.  Equilibrium under inbreeding in balanced polymorphisms.

Authors:  I Barrai; S P Mandel
Journal:  Bull World Health Organ       Date:  1971       Impact factor: 9.408

5.  Incidence of hemoglobin S carriers in Sicily.

Authors:  G Schiliro; F Di Gregorio; M A Romeo; R Testa; A Russo
Journal:  Hemoglobin       Date:  1986       Impact factor: 0.849

6.  Sicily: the world reservoir for thalassemias and haemoglobinopathies.

Authors:  G Schilirò
Journal:  Nature       Date:  1978 Dec 21-28       Impact factor: 49.962

7.  Beta-thalassemia in the Po Delta: selection, geography, and population structure.

Authors:  I Barrai; A Rosito; G Cappellozza; G Cristofori; C Vullo; C Scapoli; G Barbujani
Journal:  Am J Hum Genet       Date:  1984-09       Impact factor: 11.025

  7 in total
  4 in total

1.  Epistatic interactions between genetic disorders of hemoglobin can explain why the sickle-cell gene is uncommon in the Mediterranean.

Authors:  Bridget S Penman; Oliver G Pybus; David J Weatherall; Sunetra Gupta
Journal:  Proc Natl Acad Sci U S A       Date:  2009-12-01       Impact factor: 11.205

2.  The frequency and origin of the sickle cell mutation in the district of Coruche/Portugal.

Authors:  C Monteiro; J Rueff; A B Falcao; S Portugal; D J Weatherall; A E Kulozik
Journal:  Hum Genet       Date:  1989-06       Impact factor: 4.132

3.  Sickle cell protection from malaria.

Authors:  Sandro Eridani
Journal:  Hematol Rep       Date:  2011-11-04

Review 4.  Disease burden and quality of life of in children with sickle cell disease in Italy: time to be considered a priority.

Authors:  Raffaella Colombatti; Maddalena Casale; Giovanna Russo
Journal:  Ital J Pediatr       Date:  2021-07-29       Impact factor: 2.638

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.