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Hereditary Arterial and Articular Multiple Calcification Syndrome
A syndrome characterized by adult onset of calcification of arteries in the lower extremities and of the hand and foot capsule joints that is caused by homozygous or compound heterozygous mutation in the NT5E gene on chr
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Overview
A syndrome characterized by adult onset of calcification of arteries in the lower extremities and of the hand and foot capsule joints that is caused by homozygous or compound heterozygous mutation in the NT5E gene on chr
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