Fleck Retina of Kandori Associated with a De Novo Mutation of a Heterozygous Variant in the CAMK2A Gene

Nathalie Voide; Manon Macherel; Emmanuelle Ranza

doi:10.1055/a-2229-2877

Klinische Monatsblätter für Augenheilkunde, Table of Contents

Klin Monbl Augenheilkd 2024; 241(04): 482-484
DOI: 10.1055/a-2229-2877

Der interessante Fall

Fleck Retina of Kandori Associated with a De Novo Mutation of a Heterozygous Variant in the CAMK2A Gene

Gefleckte Retina nach Kandori ist mit einer De-novo-Mutation einer heterozygoten Variante im CAMK2A-Gen assoziiert

Authors

Nathalie Voide

¹Ophthalmology, Hopital Ophtalmique Jules Gonin, Lausanne, Switzerland
Manon Macherel

²Neuropediatrician, developmental pediatrics practice, Lausanne, Switzerland
Emmanuelle Ranza

³Medigenome, Swiss Institute of Genomic Medicine, Geneva, Switzerland

Abstract

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References

References
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