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WISP3 mutational analysis in Indian patients diagnosed with progressive pseudorheumatoid dysplasia and report of a novel mutation at p.Y198*
OBJECTIVES: To determine the pattern of mutations of the WISP3 gene in clinically identified progressive pseudorheumatoid dysplasia (PPD) in an Indian population. PATIENTS AND METHODS: A total of 15 patients with clinical features of PPD were enrolled in this study. Genomic DNA was isolated and poly...
Autores principales: | Madhuri, V., Santhanam, M., Rajagopal, K., Sugumar, L. K., Balaji, V. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4957178/ https://www.ncbi.nlm.nih.gov/pubmed/27436824 http://dx.doi.org/10.1302/2046-3758.57.2000520 |
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