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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...
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| Publicado en: | Expert Opin Orphan Drugs |
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| Autores principales: | , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
2014
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| Materias: | |
| Acceso en línea: | 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 |
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