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Rapid screening of copy number variations in STRC by droplet digital PCR in patients with mild-to-moderate hearing loss
Copy number variations (CNVs) are commonly reported in STRC, the causal gene for DFNB16. Various techniques are used clinically for CNV detection, and droplet digital PCR (ddPCR) provides highly precise absolute quantification of DNA copy number. We aimed to validate the feasibility and efficiency o...
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| Publicado no: | Hum Genome Var |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group UK
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6804619/ https://ncbi.nlm.nih.gov/pubmed/31645979 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41439-019-0075-5 |
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