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Results for Hereditary eye disease

Publications & Outputs

  1. Identification of a functionally significant tri-allelic genotype in the Tyrosinase gene (TYR) causing hypomorphic oculocutaneous albinism (OCA1B)

    Norman, C., O'Gorman, L., Gibson, J., Pengelly, R., Baralle, D., Ratnayaka, A., Griffiths, H., Rose-Zerilli, M., Ranger, M., Bunyan, D., Lee, H., Page, R., Newall, T., Shawkat, F., Mattocks, C., Ward, D., Ennis, S. & Self, J., 30/06/2017, In: Scientific Reports. 7, 9 p., 4415.

    Research output: Contribution to Journal/MagazineJournal articlepeer-review