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. 2016 Nov 25;10:2377–2382. doi: 10.2147/OPTH.S114568

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© 2016 Galantuomo et al. This work is published and licensed by Dove Medical Press Limited

The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.

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Family pedigree of an Italian family with juvenile X-linked retinoschisis from a p.Arg197Cys mutation (village of Budduso, Sardinia).

Notes: *Individuals genotyped for RS1. Unaffected individuals are represented by empty symbols. Solid squares denote affected males. Female carriers, when identified, are indicated by a shade dot inside a circle. Individuals crossed by a line represents already passed away. Each generation is identified by a Roman numeral and each individual within the same generation is numbered consecutively by an Arabic numeral. The patients are indicated by an arrow.