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Congenital microcoria deletion in mouse links Sox21 dysregulation to disease and suggests a role for TGFB2 in glaucoma and myopia.
Erjavec E, Angée C, Hadjadj D, Passet B, David P, Kostic C, Dodé E, Zanlonghi X, Cagnard N, Nedelec B, Crippa SV, Bole-Feysot C, Zarhrate M, Creuzet S, Castille J, Vilotte JL, Calvas P, Plaisancié J, Chassaing N, Kaplan J, Rozet JM, Taie LF. Erjavec E, et al. Among authors: dode e. Am J Hum Genet. 2024 Sep 13:S0002-9297(24)00305-7. doi: 10.1016/j.ajhg.2024.08.019. Online ahead of print. Am J Hum Genet. 2024. PMID: 39293448