CITATION STYLE
Yamada, Y., Nomura, N., Kitoh, H., Wakamatsu, N., & Ogasawara, N. (2000). Novel genetic mutations responsible for the HPRT deficiency and the clinical phenotypes in Japanese. In Advances in Experimental Medicine and Biology (Vol. 486, pp. 29–33). https://doi.org/10.1007/0-306-46843-3_6
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