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Neue Techniken zur Quantifizierung des Farbsinns bei Störungen der Zapfenfunktion

Huchzermeyer, Cord ; Fars, Julien ; Stöhr, Heidi ; Kremers, Jan


Background Inherited retinal diseases with cone dysfunction can be accompanied by severe visual loss and a marked loss of color vision despite relatively normal fundus appearance. Autosomal dominant occult macular dystrophy (RP1L1gene) and X-chromosomal retinitis pigmentosa (RPGRgene, including heterozygous female carriers) are important examples. New examination techniques enable quantification ...


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