HuGE Literature Finder
Records
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| High Prevalence of MYO6 Variants in an Austrian Patient Cohort With Autosomal Dominant Hereditary Hearing Loss. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2021 Mar . Frohne Alexandra, Koenighofer Martin, Liu David Tianxiang, Laccone Franco, Neesen Juergen, Gstoettner Wolfgang, Schoefer Christian, Lucas Trevor, Frei Klemens, Parzefall Thom |
| Targeted Mutation Analysis of the SLC26A4, MYO6, PJVK and CDH23 Genes in Iranian Patients with AR Nonsyndromic Hearing Loss. Fetal and pediatric pathology 2019 Apr 38 (2): 93-102. Alimardani Maliheh, Hosseini Seyed Mojtaba, Khaniani Mahmoud Shekari, Haghi Mohsen Rajati, Eslahi Atieh, Farjami Mashsa, Chezgi Javad, Derakhshan Sima Mansoori, Mojarrad Maj |
| Massively parallel DNA sequencing successfully identified seven families with deafness-associated MYO6 mutations: the mutational spectrum and clinical characteristics. The Annals of otology, rhinology, and laryngology 2015 May 124 Suppl 1 148S-57S. Miyagawa Maiko, Nishio Shin-Ya, Kumakawa Kozo, Usami Shin-Ic |
| The effect of novel mutations on the structure and enzymatic activity of unconventional myosins associated with autosomal dominant non-syndromic hearing loss. Open biology 2014 Jul 4 (7): . Kwon Tae-Jun, Oh Se-Kyung, Park Hong-Joon, Sato Osamu, Venselaar Hanka, Choi Soo Young, Kim SungHee, Lee Kyu-Yup, Bok Jinwoong, Lee Sang-Heun, Vriend Gert, Ikebe Mitsuo, Kim Un-Kyung, Choi Jae You |
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