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: | , , , , |
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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 |