Further evidence of a primary, causal association of the PTPN22 620W variant with type 1 diabetes.
Zoledziewska, Magdalena
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
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