Identification of a Novel Splice Site Mutation of theCSPG2Gene in a Japanese Family with Wagner Syndrome-Reference-Cited by-同舟云学术

Identification of a Novel Splice Site Mutation of theCSPG2Gene in a Japanese Family with Wagner Syndrome

Published:2005-08-01 Issue:8 Volume:46 Page:2726
ISSN:1552-5783
Container-title:Investigative Opthalmology & Visual Science
language:en
Short-container-title:Invest. Ophthalmol. Vis. Sci.

Author:

Miyamoto Tatsuro¹,Inoue Hiroshi²,Sakamoto Yukiko²,Kudo Eiji²,Naito Takeshi³,Mikawa Takako⁴,Mikawa Yoichi⁴,Isashiki Yasushi⁵,Osabe Dai⁶,Shinohara Shuichi⁶,Shiota Hiroshi³,Itakura Mitsuo²

Affiliation:

1. From the Division of Genetic Information, Institute for Genome Research, and the2Department of Ophthalmology and Visual Neuroscience, Institute of Health Biosciences, The University of Tokushima, Tokushima, Japan; the

2. From the Division of Genetic Information, Institute for Genome Research, and the

3. Department of Ophthalmology and Visual Neuroscience, Institute of Health Biosciences, The University of Tokushima, Tokushima, Japan; the

4. Mikawa Eye Clinic, Tokushima, Japan; the

5. Department of Ophthalmology, Kagoshima University Faculty of Medicine, Kagoshima, Japan; and the

6. Department of Bioinformatics, Division of Life Science Systems, Fujitsu, Ltd., Tokyo, Japan.

Publisher

Association for Research in Vision and Ophthalmology (ARVO)

Subject

General Medicine

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