Detailed Clinical, Ophthalmic, and Genetic Characterization of <i>MYO7A</i>-Associated Usher Syndrome
Longitudinal analysis shows that the majority of patients retain central visual function and structure until the fifth decade of life, which informs advice on prognosis and the window for therapeutic intervention.
Authors
- Angelos Kalitzeos
- Kaoru Fujinami (ORCID: https://orcid.org/0000-0003-4248-0033)
- Juan C. Romo-Aguas (ORCID: https://orcid.org/0000-0001-5293-8103)
- Yu Fujinami‐Yokokawa (ORCID: https://orcid.org/0000-0001-7555-5797)
- Anthony G. Robson (ORCID: https://orcid.org/0000-0002-8391-6123)
- Thales A. C. de Guimarães (ORCID: https://orcid.org/0000-0002-7936-6851)
- Omar A. Mahroo (ORCID: https://orcid.org/0000-0003-1254-0832)
- Chrysanthi Tsika (ORCID: https://orcid.org/0000-0001-9695-7162)
- Nancy Aychoua (ORCID: https://orcid.org/0000-0002-9514-559X)
- Michel Michaelides (ORCID: https://orcid.org/0000-0002-1552-7046)
- Andrew R. Webster (ORCID: https://orcid.org/0000-0001-6915-9560)
Institutions
- Tokyo Medical Center (JP)
- Moorfields Eye Hospital (GB)
- University College London (GB)
Publication Details
- Journal
- Investigative Ophthalmology & Visual Science
- Published
- 2025-04-21
- DOI
- https://doi.org/10.1167/iovs.66.4.60
- Citations
- 2
- Primary Topic
- Hearing, Cochlea, Tinnitus, Genetics
- Type
- article
- Field-Weighted Citation Impact
- 2.93
Funders
- Wellcome Trust
- National Institute for Health and Care Research
- Moorfields Eye Hospital NHS Foundation Trust
- Janssen Pharmaceuticals