Borate transporter SLC4A11 mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophy

Julie Desir, Graciela Moya, Orit Reish, Nicole Van Regemorter, Hilde Deconinck, Karen L. David, Françoise M. Meire, Marc J. Abramowicz*

*Corresponding author for this work

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Medicine & Life Sciences