Patient-derived cornea organoid model to study metabolomic characterization of rare disease: aniridia-associated keratopathy
Abstract Background Aniridia is a rare panocular disease caused by gene mutation in the PAX6, which is essential for eye development. Aniridia is inherited in an autosomal dominant manner, but its phenotype can vary significantly among individuals with the same mutation. Animal models, such as droso...
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Main Authors: | Ali Can Koc, Vedat Sari, Gamze Kocak, Tuba Recber, Emirhan Nemutlu, Daniel Aberdam, Sinan Güven |
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Format: | Article |
Language: | English |
Published: |
BMC
2025-01-01
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Series: | BMC Ophthalmology |
Subjects: | |
Online Access: | https://doi.org/10.1186/s12886-024-03831-w |
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