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