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Query Trace: Hearing Loss and MYO6[original query]

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 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
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 Similar articles in PubMed