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PKD2 mutation in an Iranian autosomal dominant polycystic kidney disease family with misleading linkage analysis data()
BACKGROUND: Autosomal dominant polycystic kidney disease (ADPKD) is the most common genetic renal disorder caused by mutation in 2 genes PKD1 and PKD2. Thus far, no mutation is identified in approximately 10% of ADPKD families, which can suggest further locus heterogeneity. Owing to the complexity o...
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| Publié dans: | Kidney Res Clin Pract |
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| Auteurs principaux: | , , , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Elsevier
2016
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4919558/ https://ncbi.nlm.nih.gov/pubmed/27366664 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.krcp.2016.02.003 |
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