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High Resolution Melt analysis for mutation screening in PKD1 and PKD2
BACKGROUND: Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disorder. It is characterized by focal development and progressive enlargement of renal cysts leading to end-stage renal disease. PKD1 and PKD2 have been implicated in ADPKD pathogenesis but genetic...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
BioMed Central
2011
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| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3206831/ https://ncbi.nlm.nih.gov/pubmed/22008521 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2369-12-57 |
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