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A new inbred strain JF1 established from Japanese fancy mouse carrying the classic piebald allele. <i>Mamm. Genome<\/i> 9: 15\u201319.","DOI":"10.1007\/s003359900672"},{"key":"13","doi-asserted-by":"crossref","unstructured":"13. Kumagai, T., Wada, A., Tsudzuki, M., Nishimura, M. and Kunieda, T. 1998. Nucleotide sequence of endothelin-B receptor gene reveals origin of piebald mutation in laboratory mouse. <i>Exp. Anim.<\/i> 47: 265\u2013269.","DOI":"10.1538\/expanim.47.265"},{"key":"14","doi-asserted-by":"crossref","unstructured":"14. Mori, Y., Wakamori, M., Oda, S., Fletcher, C. F., Sekiguchi, N., Mori, E., Copeland, N. G., Jenkins, N. A., Matsushita, K., Matsuyama, Z. and Imoto, K. 2000. Reduced voltage sensitivity of activation of P\/Q-type Ca<sup>2+<\/sup> channels is associated with the ataxic mouse mutation rolling Nagoya (tg(rol)). <i>J. Neurosci.<\/i> 20: 5654\u20135662.","DOI":"10.1523\/JNEUROSCI.20-15-05654.2000"},{"key":"15","doi-asserted-by":"crossref","unstructured":"15. Nagashima, K., Hisada, T., Sato, M. and Mochizuki, J. 2003. Application of new primer-enzyme combinations to terminal restriction fragment length polymorphism profiling of bacterial populations in human feces. <i>Appl. Environ. Microbiol.<\/i> 69: 1251\u20131262.","DOI":"10.1128\/AEM.69.2.1251-1262.2003"},{"key":"16","doi-asserted-by":"crossref","unstructured":"16. Oda, S. 1973. [The observation of rolling mouse Nagoya (<i>rol<\/i>), a new neurological mutant, and its maintenance (author\u2019s transl)]. <i>Jikken Dobutsu<\/i> 22: 281\u2013288.","DOI":"10.1538\/expanim1957.22.4_281"},{"key":"17","doi-asserted-by":"crossref","unstructured":"17. Pingault, V., Ente, D., Dastot-Le Moal, F., Goossens, M., Marlin, S. and Bondurand, N. 2010. Review and update of mutations causing Waardenburg syndrome. <i>Hum. Mutat.<\/i> 31: 391\u2013406.","DOI":"10.1002\/humu.21211"},{"key":"18","doi-asserted-by":"crossref","unstructured":"18. 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