Mutational analysis in sodium-borate cotransporter SLC4A11 in consanguineous families from Punjab, Pakistan
Sign Up to like & getrecommendations! Published in 2022 at "PLoS ONE"
DOI: 10.1371/journal.pone.0273685
Abstract: Aim To identify the molecular basis of Congenital Hereditary Endothelial Dystrophy CHED caused by mutations in SLC4A11, in the consanguineous Pakistani families. Methods A total of 7 consanguineous families affected with Congenital Hereditary Endothelial Dystrophy… read more here.
Keywords: slc4a11 consanguineous; sodium borate; analysis sodium; mutational analysis ... See more keywords