Genetic causes of bronchiectasis: Primary ciliary dyskinesia

Respiration

Volumn 74, Issue 3, 2007, Pages 252-263

  Morillas, Hilda N ^a,b   Zariwala, Maimoona ^a   Knowles, Michael R ^a  

^a UNIVERSITY OF NORTH CAROLINA   (United States)

^b UNIVERSITY OF NORTH CAROLINA SCHOOL OF MEDICINE   (United States)

Author keywords

Bronchiectasis; DNAH5; DNAI1; Kartagener's syndrome; Mucociliary clearance; Primary ciliary dyskinesia; Situs inversus

Indexed keywords

ANTIBIOTIC AGENT; NITRIC OXIDE; SODIUM CHLORIDE;

ALLELE; AUTOSOMAL RECESSIVE DISORDER; BRONCHIECTASIS; CHRONIC RESPIRATORY FAILURE; CILIARY DYSKINESIA; CLINICAL FEATURE; CONGENITAL HEART DISEASE; DIAGNOSTIC PROCEDURE; DIAGNOSTIC TEST; DISEASE ASSOCIATION; DNAH5 GENE; DNAI1 GENE; ENVIRONMENTAL EXPOSURE; EXERCISE; EXON; FRAMESHIFT MUTATION; GENE; GENE MUTATION; GENE SEQUENCE; GENETIC ANALYSIS; GENETIC HETEROGENEITY; GENETIC LINKAGE; GENETIC SCREENING; HETEROTAXY SYNDROME; HUMAN; LUNG INFECTION; MALE INFERTILITY; MISSENSE MUTATION; MUCOCILIARY CLEARANCE; MUTATIONAL ANALYSIS; NONSENSE MUTATION; PHENOTYPE; PHYSIOTHERAPY; POSTURAL DRAINAGE; PRIORITY JOURNAL; RESPIRATORY DISTRESS; RESPIRATORY TRACT INFECTION; REVIEW; SITUS INVERSUS; TRANSMISSION ELECTRON MICROSCOPY;

ANIMALS; BRONCHIECTASIS; CHLAMYDOMONAS REINHARDTII; CILIA; DYNEIN ATPASE; FEMALE; GENETIC HETEROGENEITY; HUMANS; INFANT, NEWBORN; KARTAGENER SYNDROME; MALE; MUTATION; PROTEINS;

EID: 34249676831     PISSN: 00257931     EISSN: None     Source Type: Journal    
DOI: 10.1159/000101783     Document Type: Review

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