Literature DB >> 2563949

One form of inclusion body beta-thalassemia is due to a GAA----TAA mutation at codon 121 of the beta chain.

Y J Fei, T A Stoming, A Kutlar, T H Huisman, G Stamatoyannopoulos.   

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Year:  1989        PMID： 2563949

Source DB:  PubMed          Journal:  Blood        ISSN： 0006-4971            Impact factor:   22.113


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  6 in total

1.  Interaction of heterozygous beta (0)-thalassemia and triplicated alpha globin loci in a Swiss-Spanish family.

Authors:  P Beris; R Darbellay; A Hochmann; E Pradervand; P Pugin
Journal:  Klin Wochenschr       Date:  1991-10-02

2.  Molecular basis for dominantly inherited inclusion body beta-thalassemia.

Authors:  S L Thein; C Hesketh; P Taylor; I J Temperley; R M Hutchinson; J M Old; W G Wood; J B Clegg; D J Weatherall
Journal:  Proc Natl Acad Sci U S A       Date:  1990-05       Impact factor: 11.205

3.  Hereditary eosinophil peroxidase deficiency: immunochemical and spectroscopic studies and evidence for a compound heterozygosity of the defect.

Authors:  M Romano; P Patriarca; C Melo; F E Baralle; P Dri
Journal:  Proc Natl Acad Sci U S A       Date:  1994-12-20       Impact factor: 11.205

4.  Association of α globin gene quadruplication and heterozygous β thalassemia in patients with thalassemia intermedia.

Authors:  Maria Carla Sollaino; Maria Elisabetta Paglietti; Lucia Perseu; Nicolina Giagu; Daniela Loi; Renzo Galanello
Journal:  Haematologica       Date:  2009-10       Impact factor: 9.941

Review 5.  The molecular basis of β-thalassemia.

Authors:  Swee Lay Thein
Journal:  Cold Spring Harb Perspect Med       Date:  2013-05-01       Impact factor: 6.915

6.  Molecular characterization of beta-thalassemia in Czechoslovakia.

Authors:  K Indrak; V Brabec; J Indrakova; L Chrobak; A Sakalova; M Jarosova; J Cermak; Y J Fei; F Kutlar; Y C Gu
Journal:  Hum Genet       Date:  1992-02       Impact factor: 4.132
  6 in total

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