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Folkerts , J., Maurer, M., Stadhouders, R., Hendricks, R., Galli, S., Tam, S.-Y., Junt , T., van IJcken, W., de Bruijn, M., van den Berg, M., Blokhuis, B., Folkerts, G., & Redegeld, F

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[4] In humans, Keutel syndrome is a rare recessive genetic disorder associated with abnormalities in the gene coding for MGP and characterized by abnormal diffuse cartilage calcification