Taylor, R. L., Handley, M. T., Waller, S., Campbell, C., Urquhart, J., Meynert, A. M., . . . Black, G. C. (2017). Novel PEX11B Mutations Extend the Peroxisome Biogenesis Disorder 14B Phenotypic Spectrum and Underscore Congenital Cataract as an Early Feature. Invest Ophthalmol Vis Sci.
Citação norma ChicagoTaylor, Rachel L., et al. "Novel PEX11B Mutations Extend the Peroxisome Biogenesis Disorder 14B Phenotypic Spectrum and Underscore Congenital Cataract As an Early Feature." Invest Ophthalmol Vis Sci 2017.
Citação norma MLATaylor, Rachel L., et al. "Novel PEX11B Mutations Extend the Peroxisome Biogenesis Disorder 14B Phenotypic Spectrum and Underscore Congenital Cataract As an Early Feature." Invest Ophthalmol Vis Sci 2017.
Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.