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The Keutel Syndrome (KS) is a rare autosomal recessive disorder that manifests in humans due to loss-of-function mutations in the MATRIX GLA PROTEIN (MGP) gene, which is correlated with ectopic calcification within cartilaginous and vascular tissues.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1505::69e01f9782eb8f136397303b892af198
https://hdl.handle.net/10400.1/19631
https://hdl.handle.net/10400.1/19631
