Lataa...
Genetics, diagnosis, and future treatment strategies for primary ciliary dyskinesia
INTRODUCTION: Primary ciliary dyskinesia (PCD) is a genetically heterogeneous recessive disorder resulting in chronic oto-sino-pulmonary disease. While PCD is estimated to occur in 1 in 20,000 individuals, fewer than 1,000 patients in the US have a well-established diagnosis. AREAS COVERED: We provi...
Tallennettuna:
| Julkaisussa: | Expert Opin Orphan Drugs |
|---|---|
| Päätekijät: | , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2014
|
| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4794317/ https://ncbi.nlm.nih.gov/pubmed/26998415 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1517/21678707.2015.989212 |
| Tagit: |
Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!
|