Literature DB >> 1675004

A StuI RFLP in the human beta-spectrin gene (SPTB).

T K Tang1, Y L Ko, W P Lien.   

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Year:  1991        PMID： 1675004      PMCID： PMC329483          DOI： 10.1093/nar/19.9.2515

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN： 0305-1048            Impact factor:   16.971


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  3 in total

1.  Assignment of the gene for beta-spectrin (SPTB) to chromosome 14q23----q24.2 by in situ hybridization.

Authors:  Y Fukushima; M G Byers; P C Watkins; J C Winkelmann; B G Forget; T B Shows
Journal:  Cytogenet Cell Genet       Date:  1990

2.  Linkage of dominant hereditary spherocytosis to the gene for the erythrocyte membrane-skeleton protein ankyrin.

Authors:  F F Costa; P Agre; P C Watkins; J C Winkelmann; T K Tang; K M John; S E Lux; B G Forget
Journal:  N Engl J Med       Date:  1990-10-11       Impact factor: 91.245

3.  Point mutation in the beta-spectrin gene associated with alpha I/74 hereditary elliptocytosis. Implications for the mechanism of spectrin dimer self-association.

Authors:  W T Tse; M C Lecomte; F F Costa; M Garbarz; C Feo; P Boivin; D Dhermy; B G Forget
Journal:  J Clin Invest       Date:  1990-09       Impact factor: 14.808
  3 in total
  1 in total

1.  Mapping the locus for familial hypertrophic cardiomyopathy to chromosome 11 in a family with a case of apical hypertrophic cardiomyopathy of the Japanese type.

Authors:  Y L Ko; J J Chen; T K Tang; M S Teng; S Y Lin; P Kuan; C W Wu; W P Lien; C C Liew
Journal:  Hum Genet       Date:  1996-04       Impact factor: 4.132
  1 in total

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