A recessive form of the Ehlers-Danlos syndrome caused by tenascin-X deficiency

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6. Deficiency of tenascin-X causes a decrease in the level of expression of type VI collagen.
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7. Recognizing the tenascin‐X deficient type of Ehlers–Danlos syndrome: a cross‐sectional study in 17 patients
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10. Elastic fiber abnormalities in hypermobility type Ehlers–Danlos syndrome patients with tenascin‐X mutations
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11. Tenascin-X: a candidate gene for benign joint hypermobility syndrome and hypermobility type Ehlers-Danlos syndrome?
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13. The Roles of Tenascins in Cardiovascular, Inflammatory, and Heritable Connective Tissue Diseases
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14. Heritable Collagen Disorders: The Paradigm of the Ehlers—Danlos Syndrome
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15. Carriership of a defective tenascin-X gene in steroid 21-hydroxylase deficiency patients: TNXB -TNXA hybrids in apparent large-scale gene conversions
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34. Tenascin-X, collagen, and Ehlers-Danlos syndrome: Tenascin-X gene defects can protect against adverse cardiovascular events
    J. Petersen, J. Douglas · 2013 · Medical Hypotheses
35. Periventricular Heterotopia: New Insights into Ehlers-Danlos Syndrome
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36. The extracellular matrix glycoprotein tenascin‐X regulates peripheral sensory and motor neurones
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37. Adrenal cortex and its disorders
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38. Homozygous Gly530Ser substitution in COL5A1 causes mild classical Ehlers‐Danlos syndrome
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41. Compound heterozygous mutations of the TNXB gene cause primary myopathy
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42. 21-Hydroxylase-Deficient Congenital Adrenal Hyperplasia
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43. Titin-based stiffening of muscle fibers in Ehlers-Danlos Syndrome
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    Chan, Angel O.K., But, W.M., Ng, K.L., Wong, L.M., Lam, Y.Y., Tiu, S.C., Lee, K.F., Lee, C.Y., Loung, P.Y., Berry, Ian R. et al. · 2011 · Steroids
46. Recurrent neuropathy associated with Ehlers–Danlos syndrome
    Nicol Cornelia Voermans, Gea Drost, A. van Kampen, A.A.W.M. Gabreëls‐Festen, Martin M. Y. Lammens, Ben C.J. Hamel, Joost Schalkwijk, Baziel G.M. van Engelen · 2005 · Journal of Neurology
47. Genes and Pseudogenes: Complexity of the RCCX Locus and Disease
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48. Muscle characteristics and altered myofascial force transmission in tenascin-X-deficient mice, a mouse model of Ehlers-Danlos syndrome
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49. Tenascin-X deficiency and Ehlers-Danlos syndrome: a case report and review of the literature
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51. Reduced quantitative muscle function in tenascin-X deficient Ehlers-Danlos patients
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53. The neuromuscular differential diagnosis of joint hypermobility
    Sandra C. Donkervoort, Carsten G. Bönnemann, Bart Loeys, Heinz Jungbluth, Nicol Cornelia Voermans · 2015 · American Journal of Medical Genetics Part C Seminars in Medical Genetics
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    Tochigi, Mamoru, Zhang, Xuan, Ohashi, Jun, Hibino, Hiroyuki, Otowa, Takeshi, Rogers, Mark, Kato, Tadafumi, Okazaki, Yuji, Kato, Nobumasa, Tokunaga, Katsushi et al. · 2007 · American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
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    E B Lee, J Y Kim, Y J Lee, Y W Song · 2005 · Annals of the Rheumatic Diseases
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99. Untitled work
    2004 · PubMed
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