Tyrosinase gene analysis in Japanese patients with oculocutaneous albinism

Author:

Goto Maki,Sato-Matsumura Kazuko C.,Sawamura Daisuke,Yokota Koichi,Nakamura Hideki,Shimizu Hiroshi

Publisher

Elsevier BV

Subject

Dermatology,Molecular Biology,Biochemistry

Reference19 articles.

1. Molecular bases of congenital hypopigmentary disorders in humans and oculocutaneous albinism 1 in Japan;Tomita;Pigment Cell Res Suppl,2000

2. Occulocutaenous albinism type1: the last 100 years;Oetting;Pigment Cell Res,2003

3. Albinism Database. Mutations of the tyrosinase gene associated with OCA1. http://www.cbc.umn.edu/tad/oca1mut.html.

4. Retina International. Mutation database, mutations of the tyrosinase gene. http://www.retina-international.org/sci-news/tyrmut.htm.

5. University of Wales College of Medicine. Human gene mutation database, Cardiff, tyrosinase gene. http://uwcmml1s.uwcm.ac.uk/uwcm/mg/search/120476.html.

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