Two novel mutations detected in Japanese patients with oculocutaneous albinism.

作者信息

Ito Shiro, Suzuki Tamio, Inagaki Katsuhiko, Suzuki Noriyuki, Kono Michihiro, Tomita Yasushi, Iwamoto Takao, Mochizuki Narutaka

出版信息

J Dermatol Sci. 2006 Nov;44(2):116-8. doi: 10.1016/j.jdermsci.2006.07.006. Epub 2006 Sep 27.

DOI:10.1016/j.jdermsci.2006.07.006

PMID:17008060

Abstract

摘要

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引用本文的文献

OCA2 481Thr, a hypofunctional allele in pigmentation, is characteristic of northeastern Asian populations.

J Hum Genet. 2007;52(8):690-693. doi: 10.1007/s10038-007-0167-9. Epub 2007 Jun 14.

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