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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:BMC Pulm Med
Autors principals: Inaba, Atsushi, Furuhata, Masanori, Morimoto, Kozo, Rahman, Mahbubur, Takahashi, Osamu, Hijikata, Minako, Knowles, Michael R., Keicho, Naoto
Format: Artigo
Idioma:Inglês
Publicat: BioMed Central 2019
Matèries:
Research Article
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
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars