LRRC6 Mutation Causes Primary Ciliary Dyskinesia with Dynein Arm Defects

Despite recent progress in defining the ciliome, the genetic basis for many cases of primary ciliary dyskinesia (PCD) remains elusive. We evaluated five children from two unrelated, consanguineous Palestinian families who had PCD with typical clinical features, reduced nasal nitric oxide concentrati...

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Detalles Bibliográficos
Autores principales: Horani, Amjad, Ferkol, Thomas W., Shoseyov, David, Wasserman, Mollie G., Oren, Yifat S., Kerem, Batsheva, Amirav, Israel, Cohen-Cymberknoh, Malena, Dutcher, Susan K., Brody, Steven L., Elpeleg, Orly, Kerem, Eitan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3602302/
https://www.ncbi.nlm.nih.gov/pubmed/23527195
http://dx.doi.org/10.1371/journal.pone.0059436

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3602302/
https://www.ncbi.nlm.nih.gov/pubmed/23527195
http://dx.doi.org/10.1371/journal.pone.0059436

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