共 120 条
- [1] Bolz HJ(2017)Next-Generation Sequencing: Quantensprung für Forschung und Diagnostik in der Ophthalmologie Klin Monbl Augenheilkd 234 280-288
- [2] Panneman DM(2023)Cost-effective sequence analysis of 113 genes in 1,192 probands with retinitis pigmentosa and Leber congenital amaurosis Front Cell Dev Biol 11 1112270-502
- [3] Hitti-Malin RJ(2022)Real-world clinical and molecular management of 50 prospective patients with microphthalmia, anophthalmia and/or ocular coloboma Br J Ophthalmol 74 489-271
- [4] Holtes LK(2023)Exome/genome sequencing in undiagnosed syndromes Annu Rev Med 23 259-1021
- [5] Harding P(2021)Clinical sites of the undiagnosed diseases network: unique contributions to genomic medicine and science Genet Med 28 1014-805
- [6] Gore S(2022)Intravitreal antisense oligonucleotide sepofarsen in Leber congenital amaurosis type 10: a phase 1b/2 trial Nat Med 11 6-826
- [7] Malka S(2022)Prevalence of RPGR-mediated retinal dystrophy in an Unselected cohort of over 5000 patients Transl Vis Sci Technol 38 799-159
- [8] Rajkumar J(2019)Association of rs613872 and trinucleotide repeat expansion in the TCF4 gene of German patients with Fuchs endothelial corneal dystrophy Cornea 119 820-2137.e2
- [9] Oluonye N(2022)Diagnostik erblicher Netzhautdystrophien. Stellenwert molekulargenetischer Diagnostik aus Patientenperspektive Ophthalmologie 34 117-74
- [10] Moosajee M(2015)IC3D classification of corneal dystrophies—edition 2 Cornea 121 2124-1385