Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: CNGA1[original query] |
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Whole exome analysis identifies frequent CNGA1 mutations in Japanese population with autosomal recessive retinitis pigmentosa. PloS one 2014 9 (9): e108721. Katagiri Satoshi, Akahori Masakazu, Sergeev Yuri, Yoshitake Kazutoshi, Ikeo Kazuho, Furuno Masaaki, Hayashi Takaaki, Kondo Mineo, Ueno Shinji, Tsunoda Kazushige, Shinoda Kei, Kuniyoshi Kazuki, Tsurusaki Yohinori, Matsumoto Naomichi, Tsuneoka Hiroshi, Iwata Takes |
Comprehensive Molecular Screening in Chinese Usher Syndrome Patients. Investigative ophthalmology & visual science 2018 Mar 59 (3): 1229-1237. Sun Tengyang, Xu Ke, Ren Yanfan, Xie Yue, Zhang Xiaohui, Tian Lu, Li Ya |
Identification of a novel homozygous variant in the CNGA1 gene in a Chinese family with autosomal recessive retinitis pigmentosa. Molecular medicine reports 2020 7 22 (3): 2516-2520. Wang Le, Zou Tongdan, Lin Yongqiong, Li Ling, Zhang Peng, Gong Bo, Hao Jilong, Zhang Houb |
Genome-wide Association Analysis Across 16,956 Patients Identifies a Novel Genetic Association Between BMP6, NIPAL1, CNGA1 and Spondylosis.
Spine 2020 Dec Publish Ahead of Print . Zhang Yanfei, Grant Ryan A, Shivakumar Manu K, Zaleski Michael, Sofoluke Nelson, Slotkin Jonathan R, Williams Marc S, Lee Ming Ta Micha |
Case Report: The First Reported Concurrence of Wilson Disease and Bilateral Retinitis Pigmentosa. Frontiers in medicine 2022 5 9 877752. Ye Zifan, Jia Xiuhua, Liu Xin, Zhang Qi, Wang Kaijun, Chen M |
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- Page last updated:Apr 29, 2024
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