Heterozygous deletion of the OPA1 gene in patients with dominant optic atrophy

被引：0
|
作者：
Takaaki Hayashi
Hiroyuki Sasano
Satoshi Katagiri
Kazushige Tsunoda
Shuhei Kameya
Mitsuru Nakazawa
Takeshi Iwata
Hiroshi Tsuneoka
机构：
[1] Katsushika Medical Center,Department of Ophthalmology, The Jikei University School of Medicine
[2] The Jikei University School of Medicine,Department of Ophthalmology
[3] National Hospital Organization Tokyo Medical Center,Laboratory of Visual Physiology, National Institute of Sensory Organs
[4] Nippon Medical School Chiba Hokusoh Hospital,Department of Ophthalmology
[5] Hirosaki University Graduate School of Medicine,Department of Ophthalmology
[6] National Hospital Organization Tokyo Medical Center,Division of Molecular and Cellular Biology, National Institute of Sensory Organs
来源：
Japanese Journal of Ophthalmology | 2017年 / 61卷
关键词：
Hereditary optic neuropathy; Genetics; Mutation;
D O I：
暂无
中图分类号：
学科分类号：
摘要：
引用
收藏
页码：395 / 401
页数：6
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