Two novel mutations involved in hereditary tyrosinemia type I.

MLA

St-Louis, M., et al. “Two Novel Mutations Involved in Hereditary Tyrosinemia Type I.” Human Molecular Genetics, vol. 4, no. 2, Feb. 1995, pp. 319–20. EBSCOhost, https://doi.org/10.1093/hmg/4.2.319.

APA

St-Louis, M., Poudrier, J., Phaneuf, D., Leclerc, B., Laframboise, R., & Tanguay, R. M. (1995). Two novel mutations involved in hereditary tyrosinemia type I. Human Molecular Genetics, 4(2), 319–320. https://doi.org/10.1093/hmg/4.2.319

Chicago

St-Louis, M, J Poudrier, D Phaneuf, B Leclerc, R Laframboise, and R M Tanguay. 1995. “Two Novel Mutations Involved in Hereditary Tyrosinemia Type I.” Human Molecular Genetics 4 (2): 319–20. doi:10.1093/hmg/4.2.319.