Matches in DBpedia 2015-10 for { ?s ?p "Camptodactyly-arthropathy-coxa vara-pericarditis syndrome is a rare genetic condition due to a mutation in the gene proteoglycan 4 (PRG4) - a chondroitin sulfate proteoglycan that acts as a lubricant for the cartilage surfaces. This gene is also known as lubricin. This condition is inherited as an autosomal recessive."@en }
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- Camptodactyly-arthropathy-coxa_vara-pericarditis_syndrome abstract "Camptodactyly-arthropathy-coxa vara-pericarditis syndrome is a rare genetic condition due to a mutation in the gene proteoglycan 4 (PRG4) - a chondroitin sulfate proteoglycan that acts as a lubricant for the cartilage surfaces. This gene is also known as lubricin. This condition is inherited as an autosomal recessive.".
- Camptodactyly-arthropathy-coxa_vara-pericarditis_syndrome comment "Camptodactyly-arthropathy-coxa vara-pericarditis syndrome is a rare genetic condition due to a mutation in the gene proteoglycan 4 (PRG4) - a chondroitin sulfate proteoglycan that acts as a lubricant for the cartilage surfaces. This gene is also known as lubricin. This condition is inherited as an autosomal recessive.".