Chronic lung disease and cystic fibrosis phenotype in prolidase deficiency: a newly recognized association.

Luder, A S; Mandel, H; Khayat, M; Gurevich, I; Frankel, P; Rivlin, J; Falik-Zaccai, T C

Luder, A S; Mandel, H; Khayat, M; Gurevich, I; Frankel, P; Rivlin, J; Falik-Zaccai, T C.

Affiliation

Luder AS; Department of Pediatrics and Genetics, Ziv Medical Center, Safed, Israel. luder@tx.technion.ac.il

J Pediatr ; 150(6): 656-8, 658.e1, 2007 Jun.

Article in En | MEDLINE | ID: mdl-17517257

Subject(s)

Cystic Fibrosis/enzymology; Dipeptidases/deficiency; Lung Diseases/enzymology; Adult; Cystic Fibrosis/genetics; Cystic Fibrosis Transmembrane Conductance Regulator/genetics; Humans; Infant; Lung Diseases/genetics; Male; Pedigree; Phenotype

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Database: MEDLINE Main subject: Cystic Fibrosis / Dipeptidases / Lung Diseases Type of study: Risk_factors_studies Limits: Adult / Humans / Infant / Male Language: En Journal: J Pediatr Year: 2007 Type: Article Affiliation country: Israel

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