Mutational analysis of theNPHP4 gene in 250 patients with nephronophthisis
Work
Year: 2005
Type: article
Abstract: Nephronophthisis (NPH), a recessive cystic kidney disease, is the most frequent genetic cause for end-stage renal disease in the first two decades of life. Mutations in three genes (NPHP1, 2, and 3) w... more
Source: Human Mutation
Institutions University of Michigan, Ludwig-Maximilians-Universität München, Max Planck Institute for Molecular Genetics, University Medical Center Freiburg
Cites: 20
Cited by: 61
Related to: 10
FWCI: 3.12
Citation percentile (by year/subfield): 95.89
Subfield: Genetics
Domain: Life Sciences
Sustainable Development Goal Good health and well-being
Open Access status: green