Human Genome Epidemiology Literature Finder
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Records 1 - 6 (of 6 Records) |
| Query Trace: Deafness and KCNQ4[original query] |
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| Identification of novel mutations in the KCNQ4 gene of patients with nonsyndromic deafness from Taiwan. Audiology & neuro-otology 2007 12 (1): 20-6. Su Ching-Chyuan, Yang Jiann-Jou, Shieh Jia-Ching, Su Mao-Chang, Li Shuan-Y |
| STRC Deletion is a Frequent Cause of Slight to Moderate Congenital Hearing Impairment in the Czech Republic. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2017 10 38 (10): e393-e400. Plevova Pavlina, Paprskarova Martina, Tvrda Petra, Turska Petra, Slavkovsky Rastislav, Mrazkova E |
| Genetic mutation of familial dilated cardiomyopathy based on next?generation semiconductor sequencing. Molecular medicine reports 2018 9 18 (5): 4271-4280. Lin Xin-Fu, Luo Jie-Wei, Liu Gui, Zhu Yao-Bin, Jin Zhao, Lin Xi |
| Genetic Aetiology of Nonsyndromic Hearing Loss in Moravia-Silesia. Medicina (Kaunas, Lithuania) 2018 10 54 (2): . Plevova Pavlina, Tvrda Petra, Paprskarova Martina, Turska Petra, Kantorova Barbara, Mrazkova Eva, Zapletalova Ja |
| A comparative analysis of genetic hearing loss phenotypes in European/American and Japanese populations. Human genetics 2020 5 139 (10): 1315-1323. Walls W Daniel, Moteki Hideaki, Thomas Taylor R, Nishio Shin-Ya, Yoshimura Hidekane, Iwasa Yoichiro, Frees Kathy L, Nishimura Carla J, Azaiez Hela, Booth Kevin T, Marini Robert J, Kolbe Diana L, Weaver A Monique, Schaefer Amanda M, Wang Kai, Braun Terry A, Usami Shin-Ichi, Barr-Gillespie Peter G, Richardson Guy P, Smith Richard J, Casavant Thomas |
| A novel KCNQ4 gene variant (c.857A>G; p.Tyr286Cys) in an extended family with non?syndromic deafness 2A. Molecular medicine reports 2021 4 23 (6): . Li Qiong, Liang Pengfei, Wang Shujuan, Li Wei, Wang Jian, Yang Yang, An Xiaogang, Chen Jun, Zha Dingj |
- Page last reviewed:Feb 1, 2024
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