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    Familial hyperinsulinism maps to chromosome 11p14–15.1, 30 cM centromeric to the insulin gene

    Familial hyperinsulinism (HI) is the most common cause of persistent neonatal hyperinsulinaemic hypoglycemia. Linkage analysis in 15 families (12 Ashkenazi Jewish, 2 consanguineous Arab, 1 non–Jewish Caucasian...

    B. Glaser, K.C. Chiu, R. Anker, A. Nestorowicz, H. Landau, H. Ben-Bassat… in Nature Genetics (1994)