Christina Gerth-Kahlert
Nov 22, 2023
Novel Mutation in Conserved Ultraviolet-Protective Tryptophan (p.Trp131Arg) Is Linked to Autosomal Dominant Congenital Cataract.
Delas F, Koller S, Feil S, Dacheva I, Gerth-Kahlert C, Berger W. Novel Mutation in Conserved Ultraviolet-Protective Tryptophan (p.Trp131Arg) Is Linked to Autosomal Dominant Congenital Cataract. Int J Mol Sci 2023; 24
Nov 22, 2023Novel Mutation in Conserved Ultraviolet-Protective Tryptophan (p.Trp131Arg) Is Linked to Autosomal Dominant Congenital Cataract.
Nov 22, 2023Int J Mol Sci 2023; 24
Delas Flora, Koller Samuel, Feil Silke, Dacheva Ivanka, Gerth-Kahlert Christina, Berger Wolfgang
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Apr 14, 2021
The "Eyelet Sign" as an MRI Clue for Inflammatory Brown Syndrome
Fierz F, Landau K, Kottke R, Wichmann W, Sturm V, Weber K, Gerth-Kahlert C. The "Eyelet Sign" as an MRI Clue for Inflammatory Brown Syndrome. J Neuroophthalmol. 2021
Apr 14, 2021The "Eyelet Sign" as an MRI Clue for Inflammatory Brown Syndrome
Apr 14, 2021J Neuroophthalmol. 2021
Fierz Fabienne C, Landau Klara, Kottke Raimund, Wichmann Werner, Sturm Veit, Weber Konrad P, Gerth-Kahlert Christina
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