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Rare heterozygous missense variants in VSX2 are associated with retinal detachment.

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Title: Rare heterozygous missense variants in VSX2 are associated with retinal detachment.
Authors: Brock, Daniel C.1,2 (AUTHOR), Dhindsa, Justin S.1,2 (AUTHOR), Chen, Yifan1,2,3,4 (AUTHOR), Ravanmehr, Vida3 (AUTHOR), Mitchell, Jonathan5 (AUTHOR), Hu, Fengyuan5 (AUTHOR), Li, Xiaoyin6 (AUTHOR), Nandigam, Likhita3 (AUTHOR), Wang, Quanli6 (AUTHOR), Wu, Kevin1 (AUTHOR), Butts, Jessica C.7 (AUTHOR), Dhindsa, Hardeep S.8 (AUTHOR), Frankfort, Benjamin J.1,9,10 (AUTHOR), Tran, Nicholas M.1 (AUTHOR), Petrovski, Slavé5,11 (AUTHOR) slav.petrovski@astrazeneca.com, Dhindsa, Ryan S.1,3,4 (AUTHOR) ryan.dhindsa@bcm.edu
Source: PLoS Genetics. 2/3/2026, Vol. 22 Issue 2, p1-25. 25p.
Database: Academic Search Ultimate
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An: 191334838
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  Data: Rare heterozygous missense variants in VSX2 are associated with retinal detachment.
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  Data: <searchLink fieldCode="JN" term="%22PLoS+Genetics%22">PLoS Genetics</searchLink>. 2/3/2026, Vol. 22 Issue 2, p1-25. 25p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=191334838
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        Value: 10.1371/journal.pgen.1012027
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              Text: 2/3/2026
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