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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Detalles Bibliográficos
Autores principales: Poprzeczko, Martyna, Bicka, Marta, Farahat, Hanan, Bazan, Rafal, Osinka, Anna, Fabczak, Hanna, Joachimiak, Ewa, Wloga, Dorota
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6952885/
https://www.ncbi.nlm.nih.gov/pubmed/31835861
http://dx.doi.org/10.3390/cells8121614

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6952885/
https://www.ncbi.nlm.nih.gov/pubmed/31835861
http://dx.doi.org/10.3390/cells8121614

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