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2, pp 500 [online] Available at: Larsson, S.C., Hakansson, N., and Wolk, A

[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

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Rebecca Tobi, the senior business and investor manager at the Food Foundation, a UK charity, says: These drugs will be hugely useful for some people, but we need to see them as treatment and not prevention