Primary ciliary dyskinesia: Critical evaluation of clinical symptoms and diagnosis in patients with normal and abnormal ultrastructure

Orphanet Journal of Rare Diseases

Volumn 9, Issue 1, 2014, Pages

  Boon, Mieke ^a   Smits, Anne ^a   Cuppens, Harry ^b   Jaspers, Martine ^a   Proesmans, Marijke ^a   Dupont, Lieven J ^a   Vermeulen, Francois L ^a   Van Daele, Sabine ^c   Malfroot, Anne ^d   Godding, Veronique ^e   Jorissen, Mark ^a   De Boeck, Kris ^a  

^a UNIVERSITY HOSPITALS LEUVEN   (Belgium)

^b UNIVERSITY OF LEUVEN   (Belgium)

^c GHENT UNIVERSITY HOSPITAL   (Belgium)

^d UNIVERSITY HOSPITAL BRUSSELS   (Belgium)

^e Hôpital Saint Luc   (Belgium)

Author keywords

DNAH11; Population characteristics; Primary cell culture; Primary ciliary dyskinesia; Transmission electron microscopy; Ultrastructure

Indexed keywords

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; CILIA; CILIARY MOTILITY DISORDERS; FEMALE; HUMANS; MALE; MICROSCOPY, ELECTRON, TRANSMISSION; RETROSPECTIVE STUDIES; YOUNG ADULT;

EID: 84892634614     PISSN: None     EISSN: 17501172     Source Type: Journal    
DOI: 10.1186/1750-1172-9-11     Document Type: Article

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