Cita APA (7a ed.)

Norman, C. S., O’Gorman, L., Gibson, J., Pengelly, R. J., Baralle, D., Ratnayaka, J. A., . . . Self, J. E. (2017). Identification of a functionally significant tri-allelic genotype in the Tyrosinase gene (TYR) causing hypomorphic oculocutaneous albinism (OCA1B). Nature Portfolio.

Cita Chicago Style (17a ed.)

Norman, Chelsea S., et al. Identification of a Functionally Significant Tri-allelic Genotype in the Tyrosinase Gene (TYR) Causing Hypomorphic Oculocutaneous Albinism (OCA1B). Nature Portfolio, 2017.

Cita MLA (8a ed.)

Norman, Chelsea S., et al. Identification of a Functionally Significant Tri-allelic Genotype in the Tyrosinase Gene (TYR) Causing Hypomorphic Oculocutaneous Albinism (OCA1B). Nature Portfolio, 2017.

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