Associated Papers
Compound Heterozygous Mutations in ZNF408 in a Patient with a Late Onset Pigmentary Retinopathy and Relatively Preserved Central Retina.
Nadelmann JB et al.
Documenta Ophthalmologica. Advances in Ophthalmology, 2021
Whole-exome sequencing reveals ZNF408 as a new gene associated with autosomal recessive retinitis pigmentosa with vitreal alterations.
Avila-Fernandez A et al.
Human Molecular Genetics, 2015
Exome sequencing confirms ZNF408 mutations as a cause of familial retinitis pigmentosa.
Habibi I et al.
Ophthalmic Genetics, 0
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