Chronic Lung Disease and Cystic Fibrosis Phenotype in Prolidase Deficiency: A Newly Recognized Association

Author:

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

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology, and Child Health

Reference11 articles.

1. Prolidase deficiency among an Israeli population: prenatal diagnosis in a genetic disorder with uncertain prognosis;Mandel;Prenat Diagn,2000

2. Prolidase deficiency;Hechtman,2001

3. Variant cystic fibrosis phenotypes in the absence of CFTR mutations;Groman;N Engl J Med,2002

4. National Institutes of Health consensus development conference statement on genetic testing for cystic fibrosis;Arch Intern Med,1999

5. Cystic fibrosis mutations in Israeli-Arab patients;Laufer-Cahana;Hum Mutat,1999

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