Variation in DNAH1 may contribute to primary ciliary dyskinesia

BACKGROUND: Primary Ciliary Dyskinesia (PCD) is a genetically heterogeneous ciliopathy caused by ultrastructural defects in ciliary or flagellar structure and is characterized by a number of clinical symptoms including recurrent respiratory infections progressing to permanent lung damage and inferti...

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Detalles Bibliográficos
Autores principales: Imtiaz, Faiqa, Allam, Rabab, Ramzan, Khushnooda, Al-Sayed, Moeenaldeen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4422061/
https://www.ncbi.nlm.nih.gov/pubmed/25927852
http://dx.doi.org/10.1186/s12881-015-0162-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4422061/
https://www.ncbi.nlm.nih.gov/pubmed/25927852
http://dx.doi.org/10.1186/s12881-015-0162-5

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