Nephronophthisis: A Genetically Diverse Ciliopathy

Nephronophthisis: A Genetically Diverse Ciliopathy

Nephronophthisis (NPHP) is an autosomal recessive cystic kidney disease and a leading genetic cause of established renal failure (ERF) in children and young adults. Early presenting symptoms in children with NPHP include polyuria, nocturia, or secondary enuresis, pointing to a urinary concentrating...

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Bibliographic Details
Main Authors:	Roslyn J. Simms, Ann Marie Hynes, Lorraine Eley, John A. Sayer
Format:	Article
Language:	English
Published:	Hindawi Limited 2011-01-01
Series:	International Journal of Nephrology
Online Access:	http://dx.doi.org/10.4061/2011/527137

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