Borate transporter SLC4A11 mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophy.
Desir J; Moya G; Reish O; Van Regemorter N; Deconinck H; David KL; Meire FM; Abramowicz MJ; Journal Of Medical Genetics, 2007, vol. 44, issue 5, p 322, ISSN 14686244. ISBN 14686244.

Full Text Resources Located for this Citation

View article on EBSCOhost(Login required)
View article via CrossRef