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Published in 2019 at "Human Mutation"
DOI: 10.1002/humu.23905
Abstract: Primary ciliary dyskinesia (PCD) is a genetically heterogeneous disease of motile cilia. Even though PCD is widely studied, NorthâAfrican patients have been rarely explored. In this study, we aim at confirming the clinical diagnosis and…
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Keywords:
primary ciliary;
ciliary dyskinesia;
pcd;
dyskinesia gene ... See more keywords