Electroretinographic anomalies in mice with mutations in Myo7a, the gene involved in human Usher syndrome type 1B.
Year: 2001
Type: article
Source: PubMed
Authors: R T Libby, K P Steel
Institution: MRC Institute of Hearing Research
Language: English
Subfield: Ophthalmology
Field: Medicine
Domain: Health Sciences
Open Access status: closed
OpenAlex ID: W1854762697