Further evidence of a primary, causal association of the PTPN22 620W variant with type 1 diabetes. [electronic resource]
Producer: 20080115Description: 229-34 p. digitalISSN:- 1939-327X
- 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
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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