Christina Gerth-Kahlert
22.11.2023
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
22.11.2023Novel Mutation in Conserved Ultraviolet-Protective Tryptophan (p.Trp131Arg) Is Linked to Autosomal Dominant Congenital Cataract.
22.11.2023Int J Mol Sci 2023; 24
Delas Flora, Koller Samuel, Feil Silke, Dacheva Ivanka, Gerth-Kahlert Christina, Berger Wolfgang
Weiter
14.04.2021
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
14.04.2021The "Eyelet Sign" as an MRI Clue for Inflammatory Brown Syndrome
14.04.2021J Neuroophthalmol. 2021
Fierz Fabienne C, Landau Klara, Kottke Raimund, Wichmann Werner, Sturm Veit, Weber Konrad P, Gerth-Kahlert Christina
Weiter