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ERG variability in X-linked congenital retinoschisis patients with mutations in the RS1 gene and the diagnostic importance of fundus autofluorescence and OCT

2007/11/06 by Agnes B. Renner, Ulrich Kellner, Britta Fiebig +4
Biochemistry, Genetics and Molecular Biology · Medicine · #Glaucoma and retinal disorders #Retinal Development and Disorders #Retinal and Macular Surgery

paper · doi:10.1007/s10633-007-9094-5

openalex publication_date 2007/11/06 · crossref created 2007/11/06 · crossref issued 2007/11/07 · crossref published 2007/11/07 · crossref published-online 2007/11/07 · crossref published-print 2008/03/01 · crossref deposited 2019/05/30 · openalex created_date 2025/10/10 · crossref indexed 2026/07/28 · openalex updated_date 2026/07/29

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