Borate transporter SLC4A 11 mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophy.
Desk, Julie; Moya, Graciela; Reish, Orit; Van Regemorter, Nkole; Deconinck, Hilde; David, Karen I.; Meire, Francoise M.; Abramowicz, Marc J.; Journal of Medical Genetics, 2007, vol. 44, issue 5, p 322, ISSN 00222593. ISBN 14686244.

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