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Abnormal properties of collagen lysyl hydroxylase from skin fibroblasts of siblings with hydroxylysine-deficient collagen.

Skin fibroblasts from two siblings with hydroxylysine-deficient collagen collagen (Ehlers-Danlos syndrome, type VI) contained normal levels of collagen prolyl hydroxylase activity but were markedly deficient in collagen lysyl hydroxylase activity. The deficiency was evident in all fractions of cell...

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Bibliografische gegevens
Gepubliceerd in:J Clin Invest
Hoofdauteurs: Quinn, R S, Krane, S M
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: American Society for Clinical Investigation 1976
Onderwerpen:
Online toegang:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC436628/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/173744/
https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI108273
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