Novel ACTG1 mutations in patients identified by massively parallel DNA sequencing cause progressive hearing loss
Work
Year: 2020
Type: article
Abstract: Human ACTG1 mutations are associated with high-frequency hearing loss, and patients with mutations in this gene are good candidates for electric acoustic stimulation. To better understand the genetic... more
Source: Scientific Reports
Institutions Shinshu University, Murata (Japan), Saitama Medical University, Toranomon Hospital, Mita Hospital +2 more
Cites: 30
Cited by: 16
Related to: 10
FWCI: 1.047
Citation percentile (by year/subfield): 57.15
Subfield: Sensory Systems
Field: Neuroscience
Domain: Life Sciences
Sustainable Development Goal Good health and well-being
Open Access status: gold
APC paid (est): $2,190
Funders Japan Agency for Medical Research and Development, Ministry of Education, Culture, Sports, Science and Technology, Ministry of Health, Labour and Welfare
Grant IDS 16kk0205010h001, 15ek0109114h001, 17H04345, H29-Nanchitou(Nan)-Ippan-031