Abstract
The Ehlers-Danlos syndrome is a heritable connective-tissue disorder caused by defects in fibrillar-collagen metabolism. Mutations in the type V collagen genes account for up to 50 percent of cases of classic Ehlers-Danlos syndrome, but many other cases are unexplained. We investigated whether the deficiency of the tenascins, extracellular-matrix proteins that are highly expressed in connective tissues, was associated with the Ehlers-Danlos syndrome.
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CITATION STYLE
Schalkwijk, J., Zweers, M. C., Steijlen, P. M., Dean, W. B., Taylor, G., van Vlijmen, I. M., … Bristow, J. (2001). A Recessive Form of the Ehlers–Danlos Syndrome Caused by Tenascin-X Deficiency. New England Journal of Medicine, 345(16), 1167–1175. https://doi.org/10.1056/nejmoa002939
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