Letter to the editor ciliary hypoplasia: A rare cause of ciliary dyskinesia

Ultrastructural Pathology

Volumn 30, Issue 5, 2006, Pages 401-402

  Gil, Yolanda Rodriguez ^a   González, Miguel Angel Martínez ^a   Orradre, Juan Luis ^b  

^a HOSPITAL UNIVERSITARIO 12 DE OCTUBRE   (Spain)

^b HOSPITAL VIRGEN DE LA SALUD   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

GLUTARALDEHYDE; DYNEIN ADENOSINE TRIPHOSPHATASE;

APLASIA; ASTHMA; CILIARY DYSKINESIA; CILIARY HYPOPLASIA; CYSTIC FIBROSIS; ELECTRON MICROSCOPY; HUMAN; HYPOPLASIA; IMMOTILE CILIA SYNDROME; IMMUNOPATHOLOGY; LETTER; LOWER RESPIRATORY TRACT; MICROVILLUS; PHENOTYPE; PRIORITY JOURNAL; RECURRENT INFECTION; RESPIRATORY TRACT DISEASE; UPPER RESPIRATORY TRACT; CASE REPORT; CHILD; ENZYMOLOGY; EUKARYOTIC FLAGELLUM; MALE; METABOLISM; MICROTUBULE; NOTE; ULTRASTRUCTURE;

CHILD; CILIA; CILIARY MOTILITY DISORDERS; DYNEIN ATPASE; HUMANS; MALE; MICROSCOPY, ELECTRON; MICROTUBULES;

EID: 33750861800     PISSN: 01913123     EISSN: 15210758     Source Type: Journal    
DOI: 10.1080/01913120600939532     Document Type: Letter

References (6)

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4. Afzelius BA. Ciliary structure in health and disease. Acta Otor Belg. 2000;54:287-291.
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6. Blouin J-L, Meeks M, Radhakrishna U, et al. Primary ciliary dyskinesia: a genome wide linkage analysis reveals extensive locus heterogenicity. Eur J Hum Genet. 2000;8:109-118.