1. Exome sequencing revealed a p.G299R mutation in the COMP gene in an Iranian family suffering from pseudoachondroplasia
   Hossein Ansari et al, 2019, The Journal of Gene Medicine CrossRef
2. Orthopaedic manifestations of pseudoachondroplasia
   D. S. Weiner et al, 2019, Journal of Children's Orthopaedics CrossRef
3. The molecular mechanism study of COMP involved in the articular cartilage damage of Kashin-Beck disease
   Mei Ma et al, 2020, Bone & Joint Research CrossRef
4. Clinical, Biochemical, Radiological, Genetic and Therapeutic Analysis of Patients with COMP Gene Variants
   Hanting Liang et al, 2022, Calcified Tissue International CrossRef