The kyphoscoliotic type of Ehlers–Danlos syndrome (type VI): differential effects on the hydroxylation of lysine in collagens I and II revealed by analysis of cross-linked telopeptides from urine
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism
Reference27 articles.
1. The Ehlers–Danlos syndrome;Steinmann,1993
2. Ehlers–Danlos syndrome: recent advances and current understanding of the clinical and genetic heterogeneity;Byers;J. Invest. Dermatol.,1994
3. Mutations in the lysyl hydroxylase 1 gene that result in enzyme deficiency and the clinical phenotype of Ehlers–Danlos syndrome type VI;Yeowell;Molec. Genet. Metabol.,2000
4. Complete genomic structure of mouse lysyl hydroxylase 2 and lysyl hydroxylase 3/collagen glucosyltransferase;Ruotsalainen;Matrix Biol.,2001
5. Tissue specificity of a new splice form of the human lysyl hydroxylase 2 gene;Yeowell;Matrix Biol.,1999
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