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Query Trace: Deafness and MYO6[original query]

Whole exome analysis of patients in Japan with hearing loss reveals high heterogeneity among responsible and novel candidate genes. Orphanet journal of rare diseases 2022 3 17 (1): 114. Mutai Hideki, Momozawa Yukihide, Kamatani Yoichiro, Nakano Atsuko, Sakamoto Hirokazu, Takiguchi Tetsuya, Nara Kiyomitsu, Kubo Michiaki, Matsunaga Tats Similar articles in PubMed
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 Similar articles in PubMed
Identification of MYO6 copy number variation associated with cochlear aplasia by targeted sequencing. International journal of pediatric otorhinolaryngology 2019 12 128 109689. Sun Lianhua, Wang Xiaowen, Hou Shule, Liang Min, Yang J Similar articles in PubMed
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 Similar articles in PubMed