| 1 | OCA1, OCA1B, OCA2, TYR
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| Mutational Analysis of the TYR and OCA2 Genes in Four Chinese Families with Oculocutaneous Albinism.
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| Wang Y, Wang Z, Chen M, Fan N, Yang J, Liu L, Wang Y, Liu X.
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| PLoS One 10(4):e0125651. doi: 10.1371/journal.pone.0125651. eCollection 2015.
2015
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| 2 | OCA1, TYR, OCA3, TYRP1, OCA1B
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| Identification of novel TYR and TYRP1 mutations in oculocutaneous albinism.
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| Forshew T, Khaliq S, Tee L, Smith U, Johnson CA, Mehdi SQ, Maher ER.
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| Clin Genet 68(2):182-4. No abstract available. 2005
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| 3 | TYR, OCA1, OCA1B
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| Molecular basis of oculocutaneous albinism type 1 in Lebanese patients.
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| Zahed L, Zahreddine H, Noureddine B, Rebeiz N, Shakar N, Zalloua P, Haddad F.
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| J Hum Genet 50(6):317-9. Epub 2005 Jun 4. 2005
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| 4 | OCA1, TYR, OCA1B
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| Leucodystrophy and oculocutaneous albinism in a child with an 11q14 deletion.
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| Coupry I, Taine L, Goizet C, Soriano C, Mortemousque B, Arveiler B, Lacombe D.
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| J Med Genet 38(1):35-8. 2001
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| 5 | TYR, OCA1, OCA1B
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| Autosomal recessive ocular albinism associated with a functionally significant tyrosinase gene polymorphism.
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| Fukai K, et al.
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| Nat Genet 9 : 92-95. 1995
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