Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Retinal Degeneration and RP2[original query] |
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Mutations in RPGR and RP2 account for 15% of males with simplex retinal degenerative disease. Investigative ophthalmology & visual science 2012 Nov . Branham K, Othman M, Brumm M, Karoukis AJ, Atmaca-Sonmez P, Yashar BM, Schwartz SB, Stover NB, Trzupek K, Wheaton D, Jennings B, Ciccarelli ML, Jayasundera KT, Lewis RA, Birch D, Bennett J, Sieving PA, Andreasson S, Duncan JL, Fishman GA, Iannaccone A, Weleber RG, Jacobson SG, Heckenlively JR, Swaroop A |
Compound pathogenic mutation in the USH2A gene in Chinese RP families detected by whole?exome sequencing. Molecular medicine reports 2018 10 18 (6): 5016-5022. Fu Yue-Chuan, Chen Na, Qiu Zi-Long, Liu Lin, Shen J |
X-linked Retinitis Pigmentosa in Japan: Clinical and Genetic Findings in Male Patients and Female Carriers. International journal of molecular sciences 2019 3 20 (6): . Kurata Kentaro, Hosono Katsuhiro, Hayashi Takaaki, Mizobuchi Kei, Katagiri Satoshi, Miyamichi Daisuke, Nishina Sachiko, Sato Miho, Azuma Noriyuki, Nakano Tadashi, Hotta Yoshihi |
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- Page last updated:Apr 29, 2024
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