Found: 2
Select item for more details and to access through your institution.
The first USH2A mutation analysis of Japanese autosomal recessive retinitis pigmentosa patients: a totally different mutation profile with the lack of frequent mutations found in Caucasian patients.
- Published in:
- Journal of Human Genetics, 2014, v. 59, n. 9, p. 521, doi. 10.1038/jhg.2014.65
- By:
- Publication type:
- Article
Bilateral multifocal retinal pigment epithelial detachments associated with abnormal multifocal electroretinograms.
- Published in:
- Japanese Journal of Ophthalmology, 2009, v. 53, n. 5, p. 556, doi. 10.1007/s10384-009-0706-3
- By:
- Publication type:
- Article