Literature DB >> 6094958

A DNA polymorphism adjacent to the human apolipoprotein CII gene.

S E Humphries, N I Jowett, L Williams, A Rees, M Vella, A Kessling, O Myklebost, A Lydon, M Seed, D J Galton.   

Abstract

We have used a cDNA clone for human apolipoprotein CII (apo CII) to detect a common DNA polymorphism with the enzyme TaqI. This polymorphism is probably caused by a single base change approximately 2000 base-pairs from the 3' end of the structural gene. In the normal population (n = 90) the frequency of the less common allele is approximately 0.44. No significant differences were observed in the allele frequency in individuals with type IIa, IIb, III, IV and V lipoprotein patterns. There does not seem to be any population association between the TaqI polymorphism and factors that predispose an individual to hyperlipidaemia.

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Year:  1983        PMID: 6094958

Source DB:  PubMed          Journal:  Mol Biol Med        ISSN: 0735-1313


  17 in total

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Authors:  L G Williams; N I Jowett; M A Vella; S Humphries; D J Galton
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Authors:  B Wainwright; M Farrall; E Watson; R Williamson
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5.  3' creatine kinase (M-type) polymorphisms linked to myotonic dystrophy in Italian and Spanish populations.

Authors:  M Gennarelli; G Novelli; A Cobo; M Baiget; B Dallapiccola
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6.  Myotonic dystrophy is closely linked to the gene for muscle-type creatine kinase (CKMM).

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7.  The 1.5-Mb region spanning the myotonic dystrophy locus shows uniform recombination frequency.

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8.  Exclusion of the Friedreich ataxia gene from chromosome 19.

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9.  A common restriction fragment length polymorphism of the human apolipoprotein E gene and its relationship to type III hyperlipidaemia.

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10.  The isolation of a genomic clone containing the apolipoprotein CII gene and the detection of linkage disequilibrium between two common DNA polymorphisms around the gene.

Authors:  S C Wallis; J A Donald; L A Forrest; R Williamson; S E Humphries
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

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