Literature DB >> 10868881

A severe clinical phenotype results from the co-inheritance of type 2 susceptibility genes and a hepatocyte nuclear factor-1alpha mutation.

C J Tack, S Ellard, A T Hattersley.   

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Year:  2000        PMID： 10868881     DOI： 10.2337/diacare.23.3.424

Source DB:  PubMed          Journal:  Diabetes Care        ISSN： 0149-5992            Impact factor:   19.112


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  1 in total

1.  Polygenic risk variants for type 2 diabetes susceptibility modify age at diagnosis in monogenic HNF1A diabetes.

Authors:  Hana Lango Allen; Stefan Johansson; Sian Ellard; Beverley Shields; Jens K Hertel; Helge Raeder; Kevin Colclough; Anders Molven; Timothy M Frayling; Pål R Njølstad; Andrew T Hattersley; Michael N Weedon
Journal:  Diabetes       Date:  2009-09-30       Impact factor: 9.461
  1 in total

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