Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Hearing and MYO1A[original query] |
---|
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 |
A genotypic ascertainment approach to refute the association of MYO1A variants with non-syndromic deafness. European journal of human genetics : EJHG 2016 Oct . Patton John, Brewer Carmen, Chien Wade, Johnston Jennifer J, Griffith Andrew J, Biesecker Leslie |
Identification of Novel PTPRQ and MYO1A Mutations in An Iranian Pedigree with Autosomal Recessive Hearing Loss. Cell journal 2018 1 20 (1): 127-131. Talebi Farah, Ghanbari Mardasi Farideh, Mohammadi Asl Javad, Tizno Saeed, Najafvand Zadeh Marzi |
Screening of noise-induced hearing loss (NIHL)-associated SNPs and the assessment of its genetic susceptibility. Environmental health : a global access science source 2019 Apr 18 (1): 30. Zhang Xuhui, Ni Yaqin, Liu Yi, Zhang Lei, Zhang Meibian, Fang Xinyan, Yang Zhangping, Wang Qiang, Li Hao, Xia Yuyong, Zhu Yim |
- Page last reviewed:Feb 1, 2024
- Page last updated:May 06, 2024
- Content source: