Levesque, S., Morin, C., Guay, S., Villeneuve, J., Marquis, P., Yik, W. Y., . . . Braverman, N. E. (2012). A founder mutation in the PEX6 gene is responsible for increased incidence of Zellweger syndrome in a French Canadian population. BioMed Central.
Trích dẫn kiểu ChicagoLevesque, Sebastien, et al. A Founder Mutation in the PEX6 Gene Is Responsible for Increased Incidence of Zellweger Syndrome in a French Canadian Population. BioMed Central, 2012.
Trích dẫn MLALevesque, Sebastien, et al. A Founder Mutation in the PEX6 Gene Is Responsible for Increased Incidence of Zellweger Syndrome in a French Canadian Population. BioMed Central, 2012.
Cảnh báo: Các trích dẫn này có thể không phải lúc nào cũng chính xác 100%.