Associated Papers
Unsuccessful transscleral cyclophotocoagulation in oculocutaneous albinism.
Dotson AD et al.
American Journal of Ophthalmology Case Reports, 2024
Identification and Computational Analysis of Novel TYR and SLC45A2 Gene Mutations in Pakistani Families With Identical Non-syndromic Oculocutaneous Albinism.
Bibi N et al.
Frontiers in Genetics, 2020
32849781 (PubMed )
Supplement: Data_Sheet_2.docx
The tyrosinase gene and oculocutaneous albinism type 1 (OCA1): A model for understanding the molecular biology of melanin formation.
Oetting WS
Pigment Cell Research, 2000
Insertion/deletion mutations of type I oculocutaneous albinism in chinese patients from Taiwan.
Tsai CH et al.
Human Mutation, 1999
Molecular basis of albinism: mutations and polymorphisms of pigmentation genes associated with albinism.
Oetting WS et al.
Human Mutation, 1999
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