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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Detalles Bibliográficos
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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Respiratory Society 2020
Materias:
Original Articles
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

Internet

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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