The polymorphism C5507G of complement receptor 1 does not explain idiopathic pulmonary fibrosis among the Finns

Respiratory Medicine

Volumn 99, Issue 3, 2005, Pages 265-267

  Hodgson, Ulla ^a,b   Tukiainen, Pentti ^a   Laitinen, Tarja ^b  

^a HELSINKI UNIVERSITY CENTRAL HOSPITAL   (Finland)

^b UNIVERSITY OF HELSINKI   (Finland)

Author keywords

Genetics; Pulmonary fibrosis

Indexed keywords

ARGININE; COMPLEMENT COMPONENT C3B RECEPTOR; PROLINE; TRYPTASE;

ADULT; AGED; ALLELE; AMINO ACID SUBSTITUTION; ARTICLE; CONTROLLED STUDY; DNA EXTRACTION; FEMALE; FIBROSING ALVEOLITIS; FINLAND; GENE SEQUENCE; GENETIC POLYMORPHISM; GENETIC PREDISPOSITION; GENETIC SUSCEPTIBILITY; GENOTYPE; HOMOZYGOSITY; HUMAN; MAJOR CLINICAL STUDY; MALE; MOLECULAR MECHANICS; PRIORITY JOURNAL; SEQUENCE ANALYSIS;

ADULT; AGED; AGED, 80 AND OVER; FEMALE; FINLAND; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HUMANS; MALE; MIDDLE AGED; POLYMORPHISM, GENETIC; PULMONARY FIBROSIS; RECEPTORS, COMPLEMENT;

EID: 13944271104     PISSN: 09546111     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.rmed.2004.08.003     Document Type: Article

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