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Summary Literature (3)
Literature for DOID 0060443: corneal endothelial dystrophy


Xenbase Articles :
( Denotes literature images)
Transmembrane water-flux through SLC4A11: a route defective in genetic corneal diseases., Vilas GL,Loganathan SK,Liu J,Riau AK,Young JD,Mehta JS,Vithana EN,Casey JR, Hum Mol Genet. November 15, 2013; 22(22):1460-2083.
Polymorphism of the LIG3 gene in keratoconus and Fuchs endothelial corneal dystrophy., Synowiec E,Wojcik KA,Izdebska J,Binczyk E,Szaflik J,Blasiak J,Szaflik JP, Cell Mol Biol (Noisy-le-grand). March 28, 2015; 61(1):0145-5680.
pH dependence of the Slc4a11-mediated H+ conductance is influenced by intracellular lysine residues and modified by disease-linked mutations., Quade BN,Marshall A,Parker MD, Am J Physiol Cell Physiol. August 1, 2020; 319(2):1522-1563.