Further evidence of a primary, causal association of the PTPN22 620W variant with type 1 diabetes. [electronic resource]
- Diabetes Jan 2008
- 229-34 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1939-327X
10.2337/db07-0289 doi
Adolescent Adult Autoimmune Diseases--genetics Child Child, Preschool DNA--blood Diabetes Mellitus, Type 1--genetics Gene Frequency Genetic Variation Genotype Humans Infant Italy Linkage Disequilibrium Polymorphism, Genetic Polymorphism, Single Nucleotide Protein Tyrosine Phosphatase, Non-Receptor Type 22--genetics Reference Values White People--genetics