Inheritance of a novel mutated allele of the OCA2 gene associated with high incidence of oculocutaneous albinism in a Polynesian community

Author:

Johanson Helene C,Chen Wei,Wicking Carol,Sturm Richard A

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Reference59 articles.

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2. King, R. A. & Oetting, W. S. Oculocutaneous albinism in The Pigmentary System—Physiology and Pathophysiology 2nd edn (eds Nordlund, J.J. et al.) (Oxford University Press, New York, 2006).

3. Oetting, W. S., Fryer, J. P., Shriram, S. & King, R. A. Oculocutaneous albinism type 1: the last 100 years. Pigment Cell Res. 16, 307–311 (2003).

4. Spritz, R. A., Chiang, P. W., Oiso, N. & Alkhateeb, A. Human and mouse disorders of pigmentation. Curr. Opin. Genet. Dev. 13, 284–289 (2003).

5. Chiang, P. W., Spector, E. & Tsai, A. C. Oculocutaneous albinism spectrum. Am. J. Med. Genet. A. 149A, 1590–1591 (2009).

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