Coincidence of PTPN22 c.1858CC and FCRL3 -169CC genotypes as a biomarker of preserved residual β-cell function in children with type 1 diabetes

Małgorzata Pawłowska , Rafał Filipów , Grzegorz Krzykowski , Anna Stanisławska-Sachadyn , Lucyna Morzuch , Julia Kulczycka , Anna Balcerska , Janusz Limon

Abstract

n/a
Author Małgorzata Pawłowska
Małgorzata Pawłowska,,
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, Rafał Filipów (FMPI / IM)
Rafał Filipów,,
- Institute of Mathematics
, Grzegorz Krzykowski (FMPI / II)
Grzegorz Krzykowski,,
- Institute of Informatics
, Anna Stanisławska-Sachadyn
Anna Stanisławska-Sachadyn,,
-
, Lucyna Morzuch
Lucyna Morzuch,,
-
, Julia Kulczycka
Julia Kulczycka,,
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, Anna Balcerska
Anna Balcerska,,
-
, Janusz Limon
Janusz Limon,,
-
Journal seriesPediatric Diabetes, ISSN 1399-543X, (A 35 pkt)
Issue year2017
Vol18
No8
Pages696-705
Publication size in sheets0.5
Keywords in Englishbiomarkers, type 1 diabetes mellitus, FCRL3 protein, human, protein tyrosine phosphatase, non-receptor type 22, sex distribution
ASJC Classification2712 Endocrinology, Diabetes and Metabolism; 2724 Internal Medicine; 2735 Pediatrics, Perinatology, and Child Health
DOIDOI:10.1111/pedi.12429
URL http://onlinelibrary.wiley.com/doi/10.1111/pedi.12429/epdf
Languageen angielski
Not used for evaluationyes
Score (nominal)0
Publication indicators Scopus SNIP (Source Normalised Impact per Paper): 2016 = 1.594; WoS Impact Factor: 2017 = 3.161 (2) - 2017=3.407 (5)
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UwagiArtykuł został zgłoszony do parametryzacji za lata 2013-2016
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