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Cited by in F6Publishing
For: Shao J, Zhao S, Yan Z, Wang L, Zhang Y, Lin M, Yu C, Wang S, Niu Y, Li X, Qiu G, Zhang J, Wu Z, Wu N; Deciphering Disorders Involving Scoliosis and COmorbidities (DISCO) study. A novel COMP mutation in a Chinese family with multiple epiphyseal dysplasia. BMC Med Genet 2020;21:115. [PMID: 32460719 DOI: 10.1186/s12881-020-01040-y] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
Number Citing Articles
1 Liang H, Hou Y, Pang Q, Jiang Y, Wang O, Li M, Xing X, Zhu H, Xia W. Clinical, Biochemical, Radiological, Genetic and Therapeutic Analysis of Patients with COMP Gene Variants. Calcif Tissue Int 2021. [PMID: 34709441 DOI: 10.1007/s00223-021-00920-6] [Reference Citation Analysis]
2 Guo BB, Jin JY, Yuan ZZ, Zeng L, Xiang R. A Novel COMP Mutated Allele Identified in a Chinese Family with Pseudoachondroplasia. Biomed Res Int 2021;2021:6678531. [PMID: 33748277 DOI: 10.1155/2021/6678531] [Reference Citation Analysis]