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Revision as of 05:09, 5 April 2024 by Maxim Masiutin(talk | contribs)(Added the cs1 style template to denote Vancouver ("vanc") citation style, because references contain "vauthors" attribute to specify the list of authors. Removed URL that duplicated identifier. Removed access-date with no URL. Removed parameters. | Use this tool. Report bugs. | #UCB_Gadget)
This gene encodes a member of von Willebrand factor A domain containing protein family. This family of proteins are thought to be involved in the formation of filamentous networks in the extracellular matrices of various tissues. Mutations of this gene have been associated with variety of inherited chondrodysplasias.[5] Three microsatellite polymorphisms in the gene, respectively consisting of 103 bp, 101 bp and 99 bp, have been linked to idiopathic scoliosis.[8]
Loughlin J, Irven C, Sykes B (1995). "Exclusion of the cartilage link protein and the cartilage matrix protein genes as the mutant loci in several heritable chondrodysplasias". Hum. Genet. 94 (6): 698–700. doi:10.1007/bf00206966. PMID7989046. S2CID30333805.