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CCN6 mutation detection in Chinese patients with progressive pseudo‐rheumatoid dysplasia and identification of four novel mutations
BACKGROUND: No formal diagnostic criteria for progressive pseudo‐rheumatoid dysplasia (PPD) are available because of insufficient clinical data, which results in that PPD is often misdiagnosed with other diseases. Whole exome sequencing (WES) and Sanger sequencing were employed to reveal the novel m...
Autores principales: | Wang, Yingjie, Xiao, Ke, Yang, Yuemei, Wu, Zhihong, Jin, Jin, Qiu, Guixing, Weng, Xisheng, Zhao, Xiuli |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7336755/ https://www.ncbi.nlm.nih.gov/pubmed/32351055 http://dx.doi.org/10.1002/mgg3.1261 |
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