A novel single nucleotide polymorphism in the protein tyrosine phosphatase N22 gene (PTPN22) is associated with Type 1 diabetes in a Chinese population - Pei, Z.; Chen, X.; Sun, C.; Du, H.; Wei, H.; Song, W.; Yang, Y.; Zhang, M.; Lu, W.; Cheng, R.; Luo, F. (Diabetic medicine, 2014)
Keywords: Asian Continental Ancestry Group - genetics; Asian Continental Ancestry Group - statistics & numerical data; Biological and medical sciences; Case-Control Studies; Child; China - epidemiology; Diabetes; Diabetes Mellitus, Type 1 - blood; Diabetes Mellitus, Type 1 - epidemiology; Diabetes Mellitus, Type 1 - genetics; Diabetes. Impaired glucose tolerance; Endocrine pancreas. Apud cells (diseases); Endocrinopathies; Etiopathogenesis. Screening. Investigations. Target tissue resistance; Feeding. Feeding behavior; Female; Fundamental and applied biological sciences. Psychology; Genetic Association Studies; Genetic Heterogeneity; Genetic Predisposition to Disease; Glycated Hemoglobin A - metabolism; Humans; Linkage Disequilibrium; Male; Medical sciences; Polymorphism, Single Nucleotide; Protein Tyrosine Phosphatase, Non-Receptor Type 22 - genetics; Vertebrates: anatomy and physiology, studies on body, several organs or systems; Vertebrates: endocrinology; Asia; China; Endocrinopathy; Human; Immunopathology; Obesity; Nutrition; Enzyme; Nutrition disorder; Phosphoric monoester hydrolases; Autoimmune disease; Metabolic diseases; Esterases; Association; Type 1 diabetes; Hydrolases; Genetics; Single nucleotide polymorphism; Protein tyrosine phosphatase nonreceptor type 2; Endocrinology; Nutritional status; Protein-tyrosine-phosphatase; PTPN22 gene