Identification of novel mutations in WISP3 gene in two unrelated Chinese families with progressive pseudorheumatoid dysplasia
Author:
Publisher
Elsevier BV
Subject
Histology,Physiology,Endocrinology, Diabetes and Metabolism
Reference21 articles.
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4. Progressive pseudorheumatoid chondrodysplasia: a report of nine cases in three families;Rezai-Delui;Skeletal. Radiol.,1994
5. The CCN family member Wisp3, mutant in progressive pseudorheumatoid dysplasia, modulates BMP and Wnt signaling;Nakamura;J. Clin. Invest.,2007
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3. Multi-scale mechanical investigation of articular cartilage suffered progressive pseudorheumatoid dysplasia;Clinical Biomechanics;2020-10
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