Publikation
Analysis of suspected Achromatopsia by multimodal Diagnostics.
Wissenschaftlicher Artikel/Review - 15.09.2023
Kugler Sylvia A, Valmaggia Christophe, Sturm Veit, Schorderet Daniel F., Todorova Margarita
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Achromatopsia (ACHM) as a hereditary cone disease might manifest in a stationary and progressive manner. The proper The primary aim of the study was to determine the spectrum of clinical and genetic diagnostics required to characterize the ACHM.The primary aim of the study was to determine the spectrum of clinical and genetic diagnostics required to characterize the ACHM.