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Sebastian Deutsch
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Autosomal Dominant Gyrate Atrophy-Like Choroidal Dystrophy Revisited: 45 Years Follow-Up and Association with a Novel <i>C1QTNF5</i> Missense Variant
by
Ulrich Kellner
,
Nicole Weisschuh
,
Silke Weinitz
,
Ghazaleh Farmand
,
Sebastian
Deutsch
,
Friederike Kortüm
,
Pascale Mazzola
,
Karin Schäferhoff
,
Valerio Marino
,
Daniele Dell’Orco
Published 2021-02-01
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