The basolateral isoform of NKCC, (NKCC1/Slc12a2 Affymetrix probe set 1367853_at), was shown to be present in a gene array of SCCD and the apical isoform (NKCC2/Slc12a1 Affymetrix probe set 1368548_at) was absent [27]. The gene discussed is SLC12A1; the disease is Schnyder corneal dystrophy.