PCD Genes—From Patients to Model Organisms and Back to Humans

Primary ciliary dyskinesia (PCD) is a hereditary genetic disorder caused by the lack of motile cilia or the assembxly of dysfunctional ones. This rare human disease affects 1 out of 10,000–20,000 individuals and is caused by mutations in at least 50 genes. The past twenty years brought significant p...

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Detalles Bibliográficos
Autores principales: Niziolek, Michal, Bicka, Marta, Osinka, Anna, Samsel, Zuzanna, Sekretarska, Justyna, Poprzeczko, Martyna, Bazan, Rafal, Fabczak, Hanna, Joachimiak, Ewa, Wloga, Dorota
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8836003/
https://www.ncbi.nlm.nih.gov/pubmed/35163666
http://dx.doi.org/10.3390/ijms23031749

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8836003/
https://www.ncbi.nlm.nih.gov/pubmed/35163666
http://dx.doi.org/10.3390/ijms23031749

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