Oculocutaneous albinism type 4: six novel mutations in the membrane-associated transporter protein gene and their phenotypes-Reference-Cited by-同舟云学术

Oculocutaneous albinism type 4: six novel mutations in the membrane-associated transporter protein gene and their phenotypes

Published:2006-10 Issue:5 Volume:19 Page:451-453
ISSN:0893-5785
Container-title:Pigment Cell Research
language:en
Short-container-title:Pigment Cell Res

Author:

Inagaki Katsuhiko,Suzuki Tamio,Ito Shiro,Suzuki Noriyuki,Adachi Koji,Okuyama Torayuki,Nakata Yusei,Shimizu Hiroshi,Matsuura Hironori,Oono Takashi,Iwamatsu Hiroko,Kono Michihiro,Tomita Yasushi

Publisher

Wiley

Subject

Cell Biology,Clinical Biochemistry,Developmental Biology,Plant Science,Agronomy and Crop Science

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0749.2006.00332.x/fullpdf

Reference12 articles.

1. Tyrosinase processing and intracellular trafficking is disrupted in mouse primary melanocytes carrying the underwhite (uw) mutation. A model for oculocutaneous albinism (OCA) type 4

2. Identification of Aim-1 as the underwhiteMouse Mutant and Its Transcriptional Regulation by MITF

3. Mutations in the gene encoding B, a novel transporter protein, reduce melanin content in medaka

4. Oculocutaneous Albinism Type 4 Is One of the Most Common Types of Albinism in Japan

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