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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...
Autores principales: | Gileles-Hillel, Alex, Mor-Shaked, Hagar, Shoseyov, David, Reiter, Joel, Tsabari, Reuven, Hevroni, Avigdor, Cohen-Cymberknoh, Malena, Amirav, Israel, Brammli-Greenberg, Shuli, Horani, Amjad, Kerem, Eitan, Breuer, Oded |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
European Respiratory Society
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7792814/ https://www.ncbi.nlm.nih.gov/pubmed/33447612 http://dx.doi.org/10.1183/23120541.00213-2020 |
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