Mutations of the XLRS1 gene cause abnormalities of photoreceptor as well as inner retinal responses of the ERG
- 1 January 1999
- journal article
- case report
- Published by Springer Nature in Documenta Ophthalmologica
- Vol. 98 (2) , 153-173
- https://doi.org/10.1023/a:1002432919073
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Positional cloning of the gene associated with X-linked juvenile retinoschisisNature Genetics, 1997
- High-Resolution Physical Map of the X-linked Retinoschisis Interval in Xp22Genomics, 1997
- X linked retinoschisis.British Journal of Ophthalmology, 1995
- Infantile presentation of X linked retinoschisis.British Journal of Ophthalmology, 1995
- Analysis of ERG a-wave amplification and kinetics in terms of the G-protein cascade of phototransduction.1994
- Experiences with the international standard for clinical electroretinography: Normative values for clinical practice, interindividual and intraindividual variations and possible extensionsDocumenta Ophthalmologica, 1993
- LINKAGE RELATIONSHIP OF X-LINKED JUVENILE RETINOSCHISIS WITH XP22.1-P22.3 PROBES1990
- X-linked congenital retinoschisisAlbrecht von Graefes Archiv für Ophthalmologie, 1990
- Psychophysical and Electroretinographic Findings in X-linked Juvenile RetinoschisisArchives of Ophthalmology (1950), 1987
- Visual acuity in 183 cases of X-chromosomal retinoschisis.1973