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Whole-exome sequencing accuracy in the diagnosis of primary ciliary dyskinesia
The diagnosis of primary ciliary dyskinesia (PCD) relies on clinical features and sophisticated studies. The detection of bi-allelic disease-causing variants confirms the diagnosis. However, a standardised genetic panel is not widely available and new disease-causing genes are continuously identifie...
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| Publicado no: | ERJ Open Res |
|---|---|
| Main Authors: | , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
European Respiratory Society
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7792814/ https://ncbi.nlm.nih.gov/pubmed/33447612 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1183/23120541.00213-2020 |
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