A Common Duplication in the Lysyl Hydroxylase Gene of Patients with Ehlers Danlos Syndrome Type VI Results in Preferential Stimulation of Lysyl Hydroxylase Activity and mRNA by Hydralazine
Author:
Publisher
Elsevier BV
Subject
Molecular Biology,Biochemistry,Biophysics
Reference32 articles.
1. The Metabolic Basis of Inherited Disease;Pinnell,1983
2. Ehlers-Danlos syndrome type VI: Clinical manifestations of collagen lysyl hydroxylase deficiency
3. A Heritable Disorder of Connective Tissue
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