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Gu, C., Yang, Z., Tan, H., Zhang, Y., Lu, Y., & Ma, Y. (2017). Decreased Plasma COMP and Increased Plasma CTX-II Levels in a Chinese Pseudoachondroplasia Family with Novel COMP Mutation. BioMed Research International, 2017, Article ID 5809787.
https://doi.org/10.1155/2017/5809787

has been cited by the following article:

• TITLE: A Chinese Family with Pseudoachondroplasia Caused by COMP Gene Mutation

  AUTHORS: Xiao Han, Yinhe Wang, Wenjin Yan, Jin Dai, Qing Jiang

  KEYWORDS: Pseudoachondroplasia, PSACH, COMP, Rhizomelic Dwarfism, Achondroplasia

  JOURNAL NAME: Advances in Anthropology, Vol.9 No.1, February 19, 2019

  ABSTRACT: Pseudoachondroplasia (PSACH; MIM 177170) is a rare disease which was characterized by disproportionate short stature, deformity of the lower limbs, brachydactyly, loose joints, and ligamentous laxity. It is an autosomal dominant osteochondrodysplasia presented in childhood, and usually resolved with age, but osteoarthritis is progressive and severe. Genetic testing using the whole exome sequencing and Sanger sequencing was performed for the patients, a 30-year-old woman and her affected son, who is only 8 years old. A heterozygous mutationin exon 15 of COMP (c.1675G > A, p.Glu559Lys, NM 000095.2) was identified. The Polyphen-2 predicted that the mutation may damage the COMP protein function. This study suggested that the heterozygous mutations in COMP were responsible for PSACH and demonstrated the genotype-phenotype relationship between mutations in COMP and clinical characteristics of PSACH.