Normal Ciliogenesis Requires Synergy between the Cystic Kidney Disease GenesMKS-3andNPHP-4
Author:
Publisher
American Society of Nephrology (ASN)
Subject
Nephrology,General Medicine
Reference45 articles.
1. Meckel-Gruber syndrome: Pathologic Manifestations, Minimal diagnostic criteria, and differential diagnosis;Alexiev;Arch Pathol Lab Med,2006
2. Pleiotropic Effects of CEP290 (NPHP6) Mutations Extend to Meckel Syndrome
3. The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome
4. A Gene for Meckel Syndrome Maps to Chromosome 11q13
5. The transmembrane protein meckelin (MKS3) is mutated in Meckel-Gruber syndrome and the wpk rat
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