Referências Bibliográficas
Todas as informações presentes nesse website/blog foram escritas com base nos seguintes artigos:
DE, Ana; YENES, Diego. El albinismo. Tipos. Etiología. Tratamiento actual y perspectivas de nuevas terapias. [s.l.: s.n., s.d.]. Disponível em: <https://repositorio.unican.es/xmlui/bitstream/handle/10902/6797/DiegoYenesAde.pdf?sequence=1>. Acesso em: 3 Jan. 2021.
Corso, Josmael & Hepp, Diego. (2013). O gene MC1R e a pigmentação dos animais. Genética na Escola. 8. 194-201.
Oetting, W.S. and King, R.A. (1999), Molecular basis of albinism: Mutations and polymorphisms of pigmentation genes associated with albinism. Hum. Mutat., 13: 99-115. https://doi.org/10.1002/(SICI)1098-1004(1999)13:2<99::AID-HUMU2>3.0.CO;2-C
Oetting, W. S. (2002). New insights into ocular albinism type 1 (OA1): Mutations and polymorphisms of the OA1 gene. Human Mutation, 19(2), 85–92. doi:10.1002/humu.10034
O'Donnell FE, Green WR, McKusick VA, Forsius H, Eriksson AW. Forsius-Eriksson syndrome: its relation to the Nettleship-Falls X-linked ocular albinism. Clin Genet. 1980 Jun;17(6):403-8. doi: 10.1111/j.1399-0004.1980.tb00170.x. PMID: 7398111.
Reetta Jalkanen, N. Torben Bech-Hansen, Rose Tobias, Eeva-Marja Sankila, Maija Mäntyjärvi, Henrik Forsius, Albert de la Chapelle, Tiina Alitalo; A Novel CACNA1F Gene Mutation Causes Åland Island Eye Disease. Invest. Ophthalmol. Vis. Sci. 2007;48(6):2498-2502. doi: https://doi.org/10.1167/iovs.06-1103.