Pawłowicz, Małgorzata <br/><br/>
Coincidence of PTPN22 c.1858CC and FCRL3 -169CC genotypes as a biomarker of preserved residual β-cell function in children with type 1 diabetes.  [electronic resource] 

 -  Pediatric diabetes  Dec 2017 
 - 696-705 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1399-5448 
<br/><br/><label>Standard No.: </label>10.1111/pedi.12429  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Child<br/>Child, Preschool<br/>Diabetes Mellitus, Type 1--blood<br/>Female<br/>Glycated Hemoglobin--metabolism<br/>Humans<br/>Infant<br/>Insulin-Secreting Cells--metabolism<br/>Longitudinal Studies<br/>Male<br/>Protein Tyrosine Phosphatase, Non-Receptor Type 22--genetics<br/>Receptors, Immunologic--genetics