Identification of novel TYR and TYRP1 mutations in oculocutaneous albinism
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2005.00460.x/fullpdf
Reference15 articles.
1. The tyrosinase gene and oculocutaneous albinism type 1 (OCA1): a model for understanding the molecular biology of melanin formation;Oetting;Pigment Cell Res,2000
2. High frequency of the Ala481Thr mutation of the P gene in the Japanese population;Suzuki;Am J Med Genet A,2003
3. Molecular basis of albinism: mutations and polymorphisms of pigmentation genes associated with albinism;Oetting;Hum Mutat,1999
4. Oculocutaneous albinism type 1: the last 100 years;Oetting;Pigment Cell Res,2003
5. The pink-eyed dilution gene and the molecular pathogenesis of tyrosinase-positive albinism (OCA2);Manga;J Dermatol,1999
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