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High‐Resolution Melt as a Screening Method in Autosomal Dominant Polycystic Kidney Disease (ADPKD)
BACKGROUND: Autosomal dominant polycystic kidney disease (ADPKD) is an inherited condition caused by PKD1 and PKD2 mutations. Complete analysis of both genes is typically required in each patient. In this study, we explored the utility of High‐Resolution Melt (HRM) as a tool for mutation analysis of...
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| Vydáno v: | J Clin Lab Anal |
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| Hlavní autoři: | , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
John Wiley and Sons Inc.
2014
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6807430/ https://ncbi.nlm.nih.gov/pubmed/24658975 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jcla.21689 |
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