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Primary ciliary dyskinesia in Japan: systematic review and meta-analysis
BACKGROUND: Primary ciliary dyskinesia (PCD) is a rare genetic disorder. Although the genetic tests and new diagnostic algorithms have recently been recommended, clinical signs and electron microscope (EM) findings have historically been the mainstays of diagnosis in Asia. To characterize PCD previo...
Guardat en:
| Publicat a: | BMC Pulm Med |
|---|---|
| Autors principals: | , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6659197/ https://ncbi.nlm.nih.gov/pubmed/31345208 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12890-019-0897-4 |
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