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C1QTNF5 missense variant causing autosomal dominant gyrate atrophy-like choroidal dystrophy.

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Bibliographic Details
Title: C1QTNF5 missense variant causing autosomal dominant gyrate atrophy-like choroidal dystrophy.
Authors: Yang-Seeger, Denise1 (AUTHOR), Pauleikhoff, Laurenz J. B.1 (AUTHOR), Atiskova, Yevgeniya1 (AUTHOR), Thiele, Sarah1 (AUTHOR), Spitzer, Martin S.1 (AUTHOR), Birtel, Johannes1,2 (AUTHOR) study-enquiry@outlook.com
Source: Ophthalmic Genetics. Aug2025, Vol. 46 Issue 4, p397-400. 4p.
Database: Academic Search Ultimate
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ISSN:13816810
DOI:10.1080/13816810.2025.2492037