Novel mutations of the GLA gene in Japanese patients with Fabry disease and their functional characterization by active site specific chaperone-Reference-Cited by-同舟云学术

Novel mutations of the GLA gene in Japanese patients with Fabry disease and their functional characterization by active site specific chaperone

Published:2008-02 Issue:2 Volume:29 Page:331-331
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Shimotori Masaaki,Maruyama Hiroki,Nakamura Gen,Suyama Takayuki,Sakamoto Fumiko,Itoh Masaaki,Miyabayashi Shigeaki,Ohnishi Takahiro,Sakai Norio,Wataya-Kaneda Mari,Kubota Mitsuru,Takahashi Toshiyuki,Mori Tatsuhiko,Tamura Katsuhiko,Kageyama Shinji,Shio Nobuo,Maeba Teruhiko,Yahagi Hirokazu,Tanaka Motoko,Oka Masayo,Sugiyama Hitoshi,Sugawara Toshiyuki,Mori Noriko,Tsukamoto Hiroko,Tamagaki Keiichi,Tanda Shuuji,Suzuki Yuka,Shinonaga Chiya,Miyazaki Jun-ichi,Ishii Satoshi,Gejyo Fumitake

Publisher

Wiley

Subject

Genetics(clinical),Genetics

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