ZMYND10 - Mutation Analysis in Slavic Patients with Primary Ciliary Dyskinesia

Primary ciliary dyskinesia (PCD) is a rare recessive disease with a prevalence of 1/10,000; its symptoms are caused by a kinetic dysfunction of motile cilia in the respiratory epithelium, flagella in spermatozoids, and primary cilia in the embryonic node. PCD is genetically heterogeneous: genotyping...

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Bibliografske podrobnosti
izdano v:PLoS One
Main Authors: Kurkowiak, Małgorzata, Ziętkiewicz, Ewa, Greber, Agnieszka, Voelkel, Katarzyna, Wojda, Alina, Pogorzelski, Andrzej, Witt, Michał
Format: Artigo
Jezik:Inglês
Izdano: Public Library of Science 2016
Teme:
Research Article
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC4732763/
https://ncbi.nlm.nih.gov/pubmed/26824761
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0148067
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