Učitavanje...
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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| Izdano u: | BMC Med Genet |
|---|---|
| Glavni autori: | , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
BioMed Central
2015
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| Teme: | |
| Online pristup: | 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 |
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