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Updated: Jan 6, 2026

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Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease
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EGFLAM Pathogenic Variants and Congenital Stationary Night Blindness
Sanja Boranijasevic1, Vasily Smirnov1,2,3, Julien Navarro1
1Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.
JAMA Ophthalmology
|December 4, 2025
Summary
Genetic variants in the EGFLAM gene cause congenital stationary night blindness (CSNB), a rare inherited retinal disorder. This finding aids in diagnosing CSNB and developing future therapies.
Area of Science:
- Ophthalmology
- Genetics
- Molecular Biology
Background:
- Congenital stationary night blindness (CSNB) is a heterogeneous inherited retinal disorder (IRD).
- Genetic causes for many complete CSNB (cCSNB) cases remain unknown.
- Identifying IRD genetic defects refines diagnostics and therapeutic development.
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