cDNA cloning and localization of OCRL-1 in rabbit kidney

The oculocerebrorenal syndrome of Lowe (OCRL) is a hereditary multisystem disorder characterized by congenital cataracts, mental retardation, renal tubular dysfunction, and progressive renal insufficiency. Tubular abnormalities include proximal tubular dysfunction, a distal acidification defect, and...

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Veröffentlicht in:	American journal of physiology. Renal physiology 1997-11, Vol.273 (5), p.F790
Hauptverfasser:	Erb, Brian C, Velázquez, Heino, Gisser, Monique, Shugrue, Christine A, Reilly, Robert F
Format:	Artikel
Sprache:	eng
Online-Zugang:	Volltext
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