Borate transporter SLC4A11 mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophy by Desir Julie, Moya Graciela, Reish Orit, Van Regemorter Nicole, Deconinck Hilde, David Karen L, Meire Françoise M, Abramowicz Marc J in Journal of medical genetics (2007).

[PMID: 17220209] PubMed

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