Albinism ocular type 1 (OA1) is an X-linked type of albinism that mainly effects pigment production in the eye, resulting in hypopigmentation of the retina, nystagmus, strabismus, foveal hypoplasia, abnormal crossing of the optic fibers, and reduced visual acuity. The OA1 gene is located on chromoso
β¦ LIBER β¦
OA1 Mutations and Deletions in X-Linked Ocular Albinism
β Scribed by Rhonda E. Schnur; Mei Gao; Penelope A. Wick; Margaret Keller; Paul J. Benke; Matthew J. Edwards; Arthur W. Grix; Athel Hockey; Jack H. Jung; Kenneth K. Kidd; Mildred Kistenmacher; Alex V. Levin; Richard A. Lewis; Maria A. Musarella; Rod W. Nowakowski; Seth J. Orlow; Roberta S. Pagon; De-Ann M. Pillers; Hope H. Punnett; Graham E. Quinn; Kamer Tezcan; Joseph Wagstaff; Richard G. Weleber
- Book ID
- 117852340
- Publisher
- American Society of Human Genetics
- Year
- 1998
- Tongue
- English
- Weight
- 234 KB
- Volume
- 62
- Category
- Article
- ISSN
- 0002-9297
- DOI
- 10.1086/301776
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