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Abstract: Nephronophthisis (NPHP) is an autosomal cystic kidney disease which is the most common hereditary disease. It is caused by mutations in 11 genes, known as nephrocystins (NPHP1-11, NPHP1L). With the identification of an increasing number of these genes, our knowledge of nephronophthisis changes and improves our comprehension of the pathomechanisms of NPHP. Ciliary expression of

Author

babu muthu

Language

EN