OpenAlex
PricingAboutJobs
Log inGet started
Work

A genotypic ascertainment approach to refute the association of MYO1A variants with non-syndromic deafness

HTML PDF

Year: 2016
Type: article
Study design: Observational Study
Source: European Journal of Human Genetics
DOI: 10.1038/ejhg.2016.140
Authors: John Patton, Carmen Brewer, Wade Chien, Jennifer J Johnston, Andrew J Griffith, Leslie G Biesecker
Institutions: National Institutes of Health, National Human Genome Research Institute, Des Moines University, National Institute on Deafness and Other Communication Disorders
Language: English

Topic: Hearing, Cochlea, Tinnitus, Genetics
Subfield: Sensory Systems
Field: Neuroscience
Domain: Life Sciences
SDG: Good health and well-being

Open Access status: bronze

Funders: National Institutes of Health, National Human Genome Research Institute
OpenAlex ID: W2533789294
FWCI: 0.99
Cites: 16
Cited by: 12
Related to: 10
OpenAlex
Nonprofit
Open DataOpen Data
Open Source
Product
Search
Compare
Pricing
Repositories
Unpaywall
Unsub
Developers
API docs
Data snapshot
Status
Source code
Organization
About
Team
Testimonials
Brand
Jobs
Community
Help center
Contact
Events
Blog
Mailing list
Supporters
Legal
Privacy
Accessibility
Terms