Novel and recurrent non-truncating mutations of the MITF basic domain: genotypic and phenotypic variations in Waardenburg and Tietz syndromes.

MLA

Léger, Sandy, et al. “Novel and Recurrent Non-Truncating Mutations of the MITF Basic Domain: Genotypic and Phenotypic Variations in Waardenburg and Tietz Syndromes.” European Journal of Human Genetics : EJHG, vol. 20, no. 5, May 2012, pp. 584–87. EBSCOhost, https://doi.org/10.1038/ejhg.2011.234.

APA

Léger, S., Balguerie, X., Goldenberg, A., Drouin-Garraud, V., Cabot, A., Amstutz-Montadert, I., Young, P., Joly, P., Bodereau, V., Holder-Espinasse, M., Jamieson, R. V., Krause, A., Chen, H., Baumann, C., Nunes, L., Dollfus, H., Goossens, M., & Pingault, V. (2012). Novel and recurrent non-truncating mutations of the MITF basic domain: genotypic and phenotypic variations in Waardenburg and Tietz syndromes. European Journal of Human Genetics : EJHG, 20(5), 584–587. https://doi.org/10.1038/ejhg.2011.234

Chicago

Léger, Sandy, Xavier Balguerie, Alice Goldenberg, Valérie Drouin-Garraud, Annick Cabot, Isabelle Amstutz-Montadert, Paul Young, et al. 2012. “Novel and Recurrent Non-Truncating Mutations of the MITF Basic Domain: Genotypic and Phenotypic Variations in Waardenburg and Tietz Syndromes.” European Journal of Human Genetics : EJHG 20 (5): 584–87. doi:10.1038/ejhg.2011.234.