Mislocalization of DNAH5 and DNAH9 in Respiratory Cells from Patients with Primary Ciliary Dyskinesia

Rationale: Primary ciliary dyskinesia (PCD) is a genetically heterogeneous disorder characterized by recurrent infections of the airways and situs inversus in half of the affected offspring. The most frequent genetic defects comprise recessive mutations of DNAH5 and DNAI1, which encode outer dynein...

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Detalhes bibliográficos
Main Authors: Fliegauf, Manfred, Olbrich, Heike, Horvath, Judit, Wildhaber, Johannes H., Zariwala, Maimoona A., Kennedy, Marcus, Knowles, Michael R., Omran, Heymut
Formato: Artigo
Idioma:Inglês
Publicado em: American Thoracic Society 2005
Assuntos:
A. Airway Biology
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2718478/
https://ncbi.nlm.nih.gov/pubmed/15750039
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1164/rccm.200411-1583OC
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