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Nephronophthisis and related syndromes
PURPOSE OF REVIEW: Nephronophthisis (NPHP) represents an autosomal recessive cystic kidney disease and is one of the most common genetic disorders causing end-stage renal disease (ESRD) in children and adolescents. NPHP is a genetically heterogenous disorder with twenty identified genes. NPHP occurs...
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| Gepubliceerd in: | Curr Opin Pediatr |
|---|---|
| Hoofdauteur: | |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
2015
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4422489/ https://ncbi.nlm.nih.gov/pubmed/25635582 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MOP.0000000000000194 |
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