Rare Human Diseases: Model Organisms in Deciphering the Molecular Basis of Primary Ciliary Dyskinesia

Primary ciliary dyskinesia (PCD) is a recessive heterogeneous disorder of motile cilia, affecting one per 15,000–30,000 individuals; however, the frequency of this disorder is likely underestimated. Even though more than 40 genes are currently associated with PCD, in the case of approximately 30% of...

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Bibliographische Detailangaben
Veröffentlicht in:Cells
Hauptverfasser: Poprzeczko, Martyna, Bicka, Marta, Farahat, Hanan, Bazan, Rafal, Osinka, Anna, Fabczak, Hanna, Joachimiak, Ewa, Wloga, Dorota
Format: Artigo
Sprache:Inglês
Veröffentlicht: MDPI 2019
Schlagworte:
Review
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6952885/
https://ncbi.nlm.nih.gov/pubmed/31835861
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/cells8121614
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