SLC4A11 and the Pathophysiology of Congenital Hereditary Endothelial Dystrophy

BioMed Research International

Volumn 2015, Issue , 2015, Pages

  Patel, Sangita P ^a,b,c   Parker, Mark D ^a,b  

^a UNIVERSITY AT BUFFALO   (United States)

^b SUNY EYE INSTITUTE   (United States)

^c VA WESTERN NEW YORK HEALTHCARE SYSTEM   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MEMBRANE PROTEIN; PROTEIN SLC4A11; SOLUTE CARRIER FAMILY 4; UNCLASSIFIED DRUG; ANION TRANSPORT PROTEIN; ANTIPORTER; GENETIC MARKER; SLC4A11 PROTEIN, HUMAN;

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CONGENITAL CORNEA DYSTROPHY; CONGENITAL GLAUCOMA; CORNEA EDEMA; CORNEA ENDOTHELIUM; ENDOTHELIUM CELL; FAMILY HISTORY; GENE MUTATION; HEARING IMPAIRMENT; HUMAN; INNER EAR; ION EXCHANGE; NONHUMAN; PATHOPHYSIOLOGY; PHENOTYPE; PROTEIN STRUCTURE; TRABECULAR MESHWORK; WATER TRANSPORT; ANIMAL; BIOLOGICAL MODEL; CHANNEL GATING; CORNEA EPITHELIUM; GENETIC MARKER; GENETIC PREDISPOSITION; GENETICS; INCIDENCE; METABOLISM; MOUSE; RISK FACTOR;

ANIMALS; ANION TRANSPORT PROTEINS; ANTIPORTERS; CORNEAL DYSTROPHIES, HEREDITARY; EPITHELIUM, CORNEAL; GENETIC MARKERS; GENETIC PREDISPOSITION TO DISEASE; HUMANS; INCIDENCE; ION CHANNEL GATING; MICE; MODELS, BIOLOGICAL; RISK FACTORS;

EID: 84942777453     PISSN: 23146133     EISSN: 23146141     Source Type: Journal    
DOI: 10.1155/2015/475392     Document Type: Article

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