Handbook of Pediatric Retinal OCT and the Eye-Brain Connection
X-linked juvenile retinoschisis
Publication
, Chapter
Ali, MH; Vajzovic, L
January 1, 2019
X-linked retinoschisis (XLRS), an inherited retinal degeneration that affects males, is caused by a mutation in the RS1 gene which encodes the protein complex retinoschisin. This chapter describes the clinical features and optical coherence tomography (OCT) characteristics of XLRS.
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Ali, M. H., & Vajzovic, L. (2019). X-linked juvenile retinoschisis. In Handbook of Pediatric Retinal OCT and the Eye-Brain Connection (pp. 119–123). https://doi.org/10.1016/B978-0-323-60984-5.00026-3
Ali, M. H., and L. Vajzovic. “X-linked juvenile retinoschisis.” In Handbook of Pediatric Retinal OCT and the Eye-Brain Connection, 119–23, 2019. https://doi.org/10.1016/B978-0-323-60984-5.00026-3.
Ali MH, Vajzovic L. X-linked juvenile retinoschisis. In: Handbook of Pediatric Retinal OCT and the Eye-Brain Connection. 2019. p. 119–23.
Ali, M. H., and L. Vajzovic. “X-linked juvenile retinoschisis.” Handbook of Pediatric Retinal OCT and the Eye-Brain Connection, 2019, pp. 119–23. Scopus, doi:10.1016/B978-0-323-60984-5.00026-3.
Ali MH, Vajzovic L. X-linked juvenile retinoschisis. Handbook of Pediatric Retinal OCT and the Eye-Brain Connection. 2019. p. 119–123.