Tenascin-X deficiency and Ehlers-Danlos syndrome: a case report and review of the literature.

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Publication year
2010Source
British Journal of Dermatology, 163, 6, (2010), pp. 1340-5ISSN
Annotation
01 december 2010
Publication type
Article / Letter to editor

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Organization
Dermatology
Journal title
British Journal of Dermatology
Volume
vol. 163
Issue
iss. 6
Page start
p. 1340
Page end
p. 5
Subject
NCMLS 1: Infection and autoimmunityAbstract
Tenascin-X is a large extracellular matrix glycoprotein that is widely distributed within connective tissues and is associated with an autosomal recessive type of Ehlers-Danlos syndrome (EDS). Tenascin-X represents the first EDS susceptibility gene that does not code for a fibrillar collagen or collagen-processing enzyme. We describe a paediatric case of tenascin-X deficiency and review the literature.
This item appears in the following Collection(s)
- Academic publications [227207]
- Electronic publications [108520]
- Faculty of Medical Sciences [86711]
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