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...

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Pubblicato in:BMC Pulm Med
Autori principali: Inaba, Atsushi, Furuhata, Masanori, Morimoto, Kozo, Rahman, Mahbubur, Takahashi, Osamu, Hijikata, Minako, Knowles, Michael R., Keicho, Naoto
Natura: Artigo
Lingua:Inglês
Pubblicazione: BioMed Central 2019
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Research Article
Accesso online: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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