CCN6 mutation detection in Chinese patients with progressive pseudo‐rheumatoid dysplasia and identification of four novel mutations-Reference-Cited by-同舟云学术

CCN6 mutation detection in Chinese patients with progressive pseudo‐rheumatoid dysplasia and identification of four novel mutations

Published:2020-04-29 Issue:7 Volume:8 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Wang Yingjie¹^ORCID,Xiao Ke²,Yang Yuemei³,Wu Zhihong³,Jin Jin¹,Qiu Guixing¹,Weng Xisheng¹,Zhao Xiuli⁴

Affiliation:

1. Department of Orthopedic Surgery Peking Union Medical College HospitalPeking Union Medical College & Chinese Academy of Medical Science Beijing China

2. Department of Orthopedic Surgery West China HospitalSichuan University Chengdu China

3. Central Laboratory Peking Union Medical College HospitalPeking Union Medical College & Chinese Academy of Medical Science Beijing China

4. Department of Medical Genetics School of Basic Medicine Peking Union Medical College Beijing China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1261

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4. An argument for early genomic sequencing in atypical cases: A WISP3 variant leads to diagnosis of progressive pseudorheumatoid arthropathy of childhood;Cassa C. A.;Rheumatology (Oxford),2016

5. Analysis of theWISP3gene in Indian families with progressive pseudorheumatoid dysplasia

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