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Journal: Int. J. Mol. Sci., 2021
Volume: 22
Number: 2089
2089
Article: Autosomal Dominant Gyrate Atrophy-Like Choroidal Dystrophy Revisited: 45 Years Follow-Up and Association with a Novel C1QTNF5 Missense Variant
Authors: by Ulrich Kellner, Nicole Weisschuh, Silke Weinitz, Ghazaleh Farmand, Sebastian Deutsch, Friederike Kortüm, Pascale Mazzola, Karin Schäferhoff, Valerio Marino and Daniele Dell’Orco
Link: https://www.mdpi.com/1422-0067/22/4/2089

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