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Cited by in F6Publishing
For: Ansari H, Mohammadi-Asl J, Hajjari M, Tahmasebi-Birgani M, Kollaee A, Jassemi-Zergani F, Vakili-Hajiagha A. Exome sequencing revealed a p.G299R mutation in the COMP gene in an Iranian family suffering from pseudoachondroplasia. J Gene Med 2019;21:e3103. [PMID: 31177591 DOI: 10.1002/jgm.3103] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
Number Citing Articles
1 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] [Cited by in F6Publishing: 2] [Reference Citation Analysis]