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See Latest ArticlesNovel mutations in cyp11b1 gene leading to 11beta-hydroxylase deficiency in brazilian patients
Journal of Clinical Endocrinology and Metabolism, 07/02/09
Mello MPD et al. - The authors describe two novel mutations, g.4671 4672insC and g.2791G>A, that drastically affects normal protein structure. These mutations abolish normal enzyme activity leading to a severe phenotype of CAH due to 11beta-hydroxylase deficiency.
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Examination of all type 2 diabetes GWAS loci reveals HHEX-IDE as a locus influencing pediatric BMI
Diabetes, 11/30/09
Reduced plasma levels of glucagon-like peptide-1 in elderly men are associated with impaired glucose tolerance but not with coronary heart disease
Diabetologia - Clinical and Experimental Diabetes and Metabolism, 11/30/09
Association of the PPARGC1A Gene Polymorphism With Diabetic Nephropathy in an Asian Indian Population (CURES-41)
Metabolic Syndrome and Related Disorders, 11/30/09
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