Cargando...
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...
Gardado en:
| Publicado en: | BMC Med Genet |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
BioMed Central
2015
|
| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4422061/ https://ncbi.nlm.nih.gov/pubmed/25927852 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-015-0162-5 |
| Tags: |
Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!
|