Hepatocyte nuclear factor 1alpha coding mutations are an uncommon contributor to early-onset type 2 diabetes in Ashkenazi Jews.

Behn, P S; Wasson, J; Chayen, S; Smolovitch, I; Thomas, J; Glaser, B; Permutt, M A

doi:10.2337/diabetes.47.6.967

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Abstract| June 01 1998

Hepatocyte nuclear factor 1alpha coding mutations are an uncommon contributor to early-onset type 2 diabetes in Ashkenazi Jews.

P S Behn;

P S Behn

Division of Metabolism, Endocrinology and Diabetes, Washington University Medical School, St. Louis, Missouri 63110, USA.

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J Wasson;

J Wasson

Division of Metabolism, Endocrinology and Diabetes, Washington University Medical School, St. Louis, Missouri 63110, USA.

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S Chayen;

S Chayen

Division of Metabolism, Endocrinology and Diabetes, Washington University Medical School, St. Louis, Missouri 63110, USA.

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I Smolovitch;

I Smolovitch

Division of Metabolism, Endocrinology and Diabetes, Washington University Medical School, St. Louis, Missouri 63110, USA.

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J Thomas;

J Thomas

Division of Metabolism, Endocrinology and Diabetes, Washington University Medical School, St. Louis, Missouri 63110, USA.

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B Glaser;

B Glaser

Division of Metabolism, Endocrinology and Diabetes, Washington University Medical School, St. Louis, Missouri 63110, USA.

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M A Permutt

Division of Metabolism, Endocrinology and Diabetes, Washington University Medical School, St. Louis, Missouri 63110, USA.

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Diabetes 1998;47(6):967–969

https://doi.org/10.2337/diabetes.47.6.967

PubMed:

9604876

Hepatocyte nuclear factor 1alpha coding mutations are an uncommon contributor to early-onset type 2 diabetes in Ashkenazi Jews.

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Hepatocyte nuclear factor 1alpha coding mutations are an uncommon contributor to early-onset type 2 diabetes in Ashkenazi Jews.

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