Research identifies CLRN1 variants in Müller cells as a cause of mitochondrial dysfunction in USH3A retinal organoids. This discovery enhances understanding of the underlying mechanisms of Usher syndrome type 3A.
clrn1 variants in m ller cells cause mitochondrial dysfunction in ush3a retinal organoids
Original title: “CLRN1 Variants in Müller Cells Cause Mitochondrial Dysfunction in USH3A Retinal Organoids.”