Literature DB >> 1911355

A spontaneous deletion of beta 33/34 Val in exon 2 of the beta globin gene (Hb Korea) produces the phenotype of dominant beta thalassaemia.

S S Park1, R Barnetson, S W Kim, D J Weatherall, S L Thein.   

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Year:  1991        PMID: 1911355     DOI: 10.1111/j.1365-2141.1991.tb04499.x

Source DB:  PubMed          Journal:  Br J Haematol        ISSN: 0007-1048            Impact factor:   6.998


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  4 in total

1.  Rapid molecular characterization of mutations leading to unstable hemoglobin beta-chain variants.

Authors:  E Girodon; N Ghanem; M Vidaud; J Riou; J Martin; F Galactéros; M Goossens
Journal:  Ann Hematol       Date:  1992-10       Impact factor: 3.673

Review 2.  Beta-thalassemia in the Korean population.

Authors:  Sung Sup Park; Han-Ik Cho
Journal:  Int J Hematol       Date:  2002-08       Impact factor: 2.490

Review 3.  The molecular basis of β-thalassemia.

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

4.  Double heterozygocity for hemoglobin C and beta thalassemia dominant: A rare case of thalassemia intermedia.

Authors:  Alexandra Agapidou; Paul King; Cecilia Ng; Dimitris A Tsitsikas
Journal:  Hematol Rep       Date:  2018-01-03
  4 in total

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