Associated Papers
A novel gene mutation in a family with X-linked retinoschisis.
Lai YH et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi, 2015
Null retinoschisin-protein expression from an RS1 c354del1-ins18 mutation causing progressive and severe XLRS in a cross-sectional family study.
Vijayasarathy C et al.
Investigative Ophthalmology & Visual Science, 2009
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