| 1 | EDSL1, TNXB
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| Phenotypic effects of Ehlers-Danlos syndrome-associated mutation on the FnIII domain of tenascin-X.
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| Zhuang S, Linhananta A, Li H.
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| Protein Sci 19(11):2231-9.
2010
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| 2 | EDSL1, TNXB
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| Muscle characteristics and altered myofascial force transmission in tenascin-X-deficient mice, a mouse model of Ehlers-Danlos syndrome.
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| Huijing PA, Voermans NC, Baan GC, Busé TE, van Engelen BG, de Haan A.
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| J Appl Physiol 109(4):986-95. Epub 2010 Jun 24.
2010
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| 3 | TNXB, EDSL1
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| Elastic fiber abnormalities in hypermobility type Ehlers-Danlos syndrome patients with tenascin-X mutations.
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| Zweers MC, Dean WB, van Kuppevelt TH, Bristow J, Schalkwijk J.
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| Clin Genet 67(4):330-4. 2005
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| 4 | TNXB, EDSL1
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| Deficiency of tenascin-X causes abnormalities in dermal elastic fiber morphology.
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| Zweers MC, van Vlijmen-Willems IM, van Kuppevelt TH, Mecham RP, Steijlen PM, Bristow J, Schalkwijk J.
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| J Invest Dermatol 122(4):885-91. 2004
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| 5 | EDSL1, TNXB
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| A recessive form of the Ehlers-Danlos syndrome caused by tenascin-X deficiency.
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| Schalkwijk J, Zweers MC, Steijlen PM, Dean WB, Taylor G, van Vlijmen IM, van Haren B, Miller WL, Bristow J.
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| N Engl J Med 345(16):1167-75. 2001
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| 6 | EDSL1, TNXB
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| Tenascin-X deficiency is associated with Ehlers-Danlos syndrome.
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| Burch GH, Gong Y, Liu W, Dettman RW, Curry CJ, Smith L, Miller WL, Bristow J.
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| Nat Genet 17(1):104-8. 1997
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