Title : Human dermatosparaxis: a form of Ehlers-Danlos syndrome that results from failure to remove the amino-terminal propeptide of type I procollagen.

Pub. Date : 1992 Aug

PMID : 1642226






2 Functional Relationships(s)
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1 Dermatosparaxis is a recessively inherited connective-tissue disorder that results from lack of the activity of type I procollagen N-proteinase, the enzyme that removes the amino-terminal propeptides from type I procollagen. propeptides collagen type I alpha 2 chain Homo sapiens
2 Dermatosparaxis is a recessively inherited connective-tissue disorder that results from lack of the activity of type I procollagen N-proteinase, the enzyme that removes the amino-terminal propeptides from type I procollagen. propeptides collagen type I alpha 2 chain Homo sapiens