Autosomal Dominant Gyrate Atrophy-Like Choroidal Dystrophy Revisited: 45 Years Follow-Up and Association with a Novel C1QTNF5 Missense Variant

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Autosomal Dominant Gyrate Atrophy-Like Choroidal Dystrophy Revisited: 45 Years Follow-Up and Association with a Novel C1QTNF5 Missense Variant

Author: Kellner, Ulrich; Weisschuh, Nicole; Weinitz, Silke; Farmand, Ghazaleh; Deutsch, Sebastian; Kortum, Friederike; Mazzola, Pascale; Schaferhoff, Karin; Marino, Valerio; Dell'Orco, Daniele
Tübinger Autor(en):
Weisschuh, Nicole
Mazzola, Pascale
Kortüm, Friederike Charlotte Christina
Schäferhoff, Karin
Published in: International Journal of Molecular Sciences (2021), Bd. 22 (4), Article 2089
Verlagsangabe: Mdpi
Language: English
Full text: http://dx.doi.org/10.3390/ijms22042089
ISSN: 1422-0067
DDC Classifikation: 540 - Chemistry and allied sciences
570 - Life sciences; biology
Dokumentart: Article
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