The role of PTPN22 C1858T gene polymorphism in diabetes mellitus type 1: First evaluation in greek children and adolescents

BioMed Research International

Volumn 2013, Issue , 2013, Pages

  Giza, Styliani ^a   Goulas, Antonios ^a   Gbandi, Emmanouela ^a   Effraimidou, Smaragda ^b   Papadopoulou Alataki, Efimia ^a   Eboriadou, Maria ^a   Galli Tsinopoulou, Assimina ^a  

^a ARISTOTLE UNIVERSITY OF THESSALONIKI   (Greece)

^b PAPAGEORGIOU GENERAL HOSPITAL   (Greece)

Author keywords

[No Author keywords available]

Indexed keywords

NON RECEPTOR PROTEIN TYROSINE PHOSPHATASE 22; PTPN22 PROTEIN, HUMAN;

ADOLESCENT; ADOLESCENT DISEASE; ALLELE; ARTICLE; CHILD; CONTROLLED STUDY; DIABETIC KETOACIDOSIS; DNA POLYMORPHISM; FAMILY HISTORY; FEMALE; GENETIC ASSOCIATION; GENOTYPE; GREECE; HASHIMOTO DISEASE; HUMAN; INSULIN DEPENDENT DIABETES MELLITUS; MAJOR CLINICAL STUDY; MALE; POLYMERASE CHAIN REACTION; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SCHOOL CHILD; GENE FREQUENCY; GENETIC PREDISPOSITION; GENETICS; PATHOLOGY; SINGLE NUCLEOTIDE POLYMORPHISM;

ADOLESCENT; ALLELES; CHILD; DIABETES MELLITUS, TYPE 1; FEMALE; GENE FREQUENCY; GENETIC ASSOCIATION STUDIES; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HUMANS; MALE; POLYMORPHISM, SINGLE NUCLEOTIDE; PROTEIN TYROSINE PHOSPHATASE, NON-RECEPTOR TYPE 22;

EID: 84881513450     PISSN: 23146133     EISSN: 23146141     Source Type: Journal    
DOI: 10.1155/2013/721604     Document Type: Article

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