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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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| Publicado no: | PLoS One |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2016
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| Assuntos: | |
| Acesso em linha: | 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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