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Exome sequencing in a swiss childhood glaucoma cohort reveals CYP1B1 and FOXC1 variants as most frequent causes
Elena Lang, Samuel Koller, Luzy Bähr, Marc Töteberg-Harms, David Atac, Françoise Roulez, Angela Bahr, Katharina Steindl, Silke Feil, Wolfgang Berger, Christina Gerth-Kahlert
Research output: Contribution to journal › Article › peer-review
15
Scopus
citations