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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...

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Main Authors: Lejla Pojskic, Ismet Gavrankapetanovic, Naida Lojo-Kadric, Rifat Hadziselimovic, Kasim Bajrovic
Format: Artigo
Language:Inglês
Published: University of Sarajevo 2015-09-01
Series:Journal of Health Sciences
Subjects:
Progressive pseudorheumatoid dysplasia (PPD)
genetic diagnosis
WISP3 mutation
familial mutation
Online Access:https://www.jhsci.ba/ojs/index.php/jhsci/article/view/394
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