Seeing in Color: Inclusion and Characterization of Hereditary Eye Disease in African Americans

Author:

Owete Agnes C.12,Ionin Raisa3,Huryn Laryssa A.1,Cukras Catherine A.1,Blain Delphine1,Agather Aime R.1,Hufnagel Robert B.1,Brooks Brian P.1,Nwanyanwu Kristen4,Zein Wadih M.1

Affiliation:

1. Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institute of Health, Bethesda, MD, USA

2. Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA

3. National Institutes of Health Library, National Institutes of Health, Bethesda, MD, USA

4. Department of Ophthalmology and Visual Science, Yale School of Medicine, New Haven, CT, USA

Publisher

Association for Research in Vision and Ophthalmology (ARVO)

Reference54 articles.

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2. Diversity and inclusion in genomic research: why the uneven progress?;Bentley;J Community Genet,2017

3. African origin of an intragenic deletion of the human P gene in tyrosinase positive oculocutaneous albinism;Durham-Pierre;Nat Genet,1994

4. Diverse mutations of the P gene among African-Americans with type II (tyrosinase-positive) oculocutaneous albinism (OCA2);Lee;Hum Mol Genet,1994

5. An intragenic deletion of the P gene is the common mutation causing tyrosinase-positive oculocutaneous albinism in southern African Negroids;Stevens;Am J Hum Genet,1995

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