A genotyping assay for missense mutation in WISP3 gene associated with childhood onset pseudorheumatoid arthropathy
Introduction: Progressive pseudorheumatoid dysplasia (PPD) is an autosomal recessive genetic disorder reported to be caused by gene alterations of the Wnt1-inducible signaling pathway protein 3 corresponding gene (WISP3) located on chromosome position 6q22. Up to date, there is only a handful of WI...
Main Authors: | Lejla Pojskic, Ismet Gavrankapetanovic, Naida Lojo-Kadric, Rifat Hadziselimovic, Kasim Bajrovic |
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Format: | Article |
Language: | English |
Published: |
University of Sarajevo
2015-09-01
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Series: | Journal of Health Sciences |
Subjects: | |
Online Access: | https://www.jhsci.ba/ojs/index.php/jhsci/article/view/394 |
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