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Anthony, J. B. and Ramesh, C. T. 1997. The cornea and sclera. pp. 233\u2013278. <i>In<\/i>: Wolff\u2019s Anatomy of the Eye and Orbit, 8th ed., Chapman &amp; Hall, London."},{"key":"2","doi-asserted-by":"crossref","unstructured":"2. Bin, B. H., Fukada, T., Hosaka, T., Yamasaki, S., Ohashi, W., Hojyo, S., Miyai, T., Nishida, K., Yokoyama, S. and Hirano, T. 2011. Biochemical characterization of human ZIP13 protein: a homo-dimerized zinc transporter involved in the spondylocheiro dysplastic Ehlers-Danlos syndrome. <i>J. Biol. Chem.<\/i> 286: 40255\u201340265.","DOI":"10.1074\/jbc.M111.256784"},{"key":"3","doi-asserted-by":"crossref","unstructured":"3. Bin, B. H., Hojyo, S., Hosaka, T., Bhin, J., Kano, H., Miyai, T., Ikeda, M., Kimura-Someya, T., Shirouzu, M., Cho, E. G., Fukue, K., Kambe, T., Ohashi, W., Kim, K. H., Seo, J., Choi, D. H., Nam, Y. J., Hwang, D., Fukunaka, A., Fujitani, Y., Yokoyama, S., Superti-Furga, A., Ikegawa, S., Lee, T. R. and Fukada, T. 2014. Molecular pathogenesis of spondylocheirodysplastic Ehlers-Danlos syndrome caused by mutant ZIP13 proteins. <i>EMBO Mol. Med.<\/i> 6: 1028\u20131042.","DOI":"10.15252\/emmm.201303809"},{"key":"4","unstructured":"4. Castori, M. and Voermans, N. C. 2014. Neurological manifestations of Ehlers-Danlos syndrome(s): A review. <i>Iran. J. Neurol.<\/i> 13: 190\u2013208."},{"key":"5","doi-asserted-by":"crossref","unstructured":"5. Chakravarti, S., Magnuson, T., Lass, J. H., Jepsen, K. J., LaMantia, C. and Carroll, H. 1998. Lumican regulates collagen fibril assembly: skin fragility and corneal opacity in the absence of lumican. <i>J. Cell Biol.<\/i> 141: 1277\u20131286.","DOI":"10.1083\/jcb.141.5.1277"},{"key":"6","unstructured":"6. Deren-Wagemann, I., Kuliszkiewicz-Janus, M. and Schiller, J. 2010. The ehlers-danlos syndrome. <i>Adv. Exp. Med. Biol.<\/i> 19: 537\u2013542."},{"key":"7","doi-asserted-by":"crossref","unstructured":"7. Fukada, T., Civic, N., Furuichi, T., Shimoda, S., Mishima, K., Higashiyama, H., Idaira, Y., Asada, Y., Kitamura, H., Yamasaki, S., Hojyo, S., Nakayama, M., Ohara, O., Koseki, H., Dos Santos, H. G., Bonafe, L., Ha-Vinh, R., Zankl, A., Unger, S., Kraenzlin, M. E., Beckmann, J. S., Saito, I., Rivolta, C., Ikegawa, S., Superti-Furga, A. and Hirano, T. 2008. The zinc transporter SLC39A13\/ZIP13 is required for connective tissue development; its involvement in BMP\/TGF-\u03b2 signaling pathways. <i>PLoS ONE<\/i> 3: e3642.","DOI":"10.1371\/journal.pone.0003642"},{"key":"8","doi-asserted-by":"crossref","unstructured":"8. Hara, T., Takeda, T. A., Takagishi, T., Fukue, K., Kambe, T. and Fukada, T. 2017. Physiological roles of zinc transporters: molecular and genetic importance in zinc homeostasis. <i>J. Physiol. Sci.<\/i> 67: 283\u2013301.","DOI":"10.1007\/s12576-017-0521-4"},{"key":"9","doi-asserted-by":"crossref","unstructured":"9. Hilbert, L., Sata, Y., Kimura, H., Julicher, F., Honigmann, A., Zaburdaev, V. and Vastenhouw, N. 2017. Transcription establishes microenvironments that organize euchromatin. <i>bioRxiv<\/i>: doi: 10.1101\/234112.","DOI":"10.1101\/234112"},{"key":"10","doi-asserted-by":"crossref","unstructured":"10. Hirose, T., Ogura, T., Tanaka, K., Minaguchi, J., Yamauchi, T., Fukada, T., Koyama, Y. and Takehana, K. 2015. Comparative study of dermal components and plasma TGF-\u03b21 levels in Slc39a13\/<i>Zip13<\/i>-KO mice. <i>J. Vet. Med. Sci.<\/i> 77: 1385\u20131389.","DOI":"10.1292\/jvms.15-0015"},{"key":"11","unstructured":"11. Hogan, M. J., Alvarado, J. A. and Weddell, J. E. 1971. Histology of the Human Eye. Saunders, Philadelphia."},{"key":"12","doi-asserted-by":"crossref","unstructured":"12. Iwasaki, S., Hosaka, Y., Iwasaki, T., Yamamoto, K., Nagayasu, A., Ueda, H., Kokai, Y. and Takehana, K. 2008. The modulation of collagen fibril assembly and its structure by decorin: an electron microscopic study. <i>Arch. Histol. Cytol.<\/i> 71: 37\u201344.","DOI":"10.1679\/aohc.71.37"},{"key":"13","doi-asserted-by":"crossref","unstructured":"13. Malfait, F., Francomano, C., Byers, P., Belmont, J., Berglund, B., Black, J., Bloom, L., Bowen, J. M., Brady, A. F., Burrows, N. P., Castori, M., Cohen, H., Colombi, M., Demirdas, S., De Backer, J., De Paepe, A., Fournel-Gigleux, S., Frank, M., Ghali, N., Giunta, C., Grahame, R., Hakim, A., Jeunemaitre, X., Johnson, D., Juul-Kristensen, B., Kapferer-Seebacher, I., Kazkaz, H., Kosho, T., Lavallee, M. E., Levy, H., Mendoza-Londono, R., Pepin, M., Pope, F. M., Reinstein, E., Robert, L., Rohrbach, M., Sanders, L., Sobey, G. J., Van Damme, T., Vandersteen, A., van Mourik, C., Voermans, N., Wheeldon, N., Zschocke, J. and Tinkle, B. 2017. The 2017 international classification of the Ehlers-Danlos syndromes. <i>Am. J. Med. Genet. C. Semin. Med. 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