The Pink-Eyed Dilution Gene and the Molecular Pathogenesis of Tyrosinase-Positive Albinism (OCA2)
Author:
Affiliation:
1. The Ronald O. Perelman Department of Dermatology & The Department of Cell Biology; NYU School of Medicine; New York NY 10016 U.S.A.
Publisher
Wiley
Subject
Dermatology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1346-8138.1999.tb02085.x/fullpdf
Reference80 articles.
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2. Human oculocutaneous albinism caused by single base insertion in the tyrosinase gene;Tomita;Biochem biophys Res Commun,1989
3. Molecular basis of type I (tyrosinase-related) oculocutaneous albinism: Mutations and polymorphisms of the human tyrosinase gene;Oetting;Hum Mutat,1993
4. Partial purification and kinetic studies of mammalian tyrosinase;Shimano;Biochem Biophys Acta,1962
5. Mutational mapping of the catalytic activities of human tyrosinase;Tripathi;J Biol Chem,1992
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