A Pilot Survey of Cystic Fibrosis Clinical Manifestations in CFTR Mutation Heterozygotes
Author:
Affiliation:
1. Cystic Fibrosis Center, Azienda Ospedaliera Verona, Verona, Italy
Publisher
Mary Ann Liebert Inc
Subject
Genetics (clinical)
Link
http://www.liebertpub.com/doi/pdf/10.1089/10906570152742317
Reference15 articles.
1. Clinical presentation of exclusive cystic fibrosis lung disease
2. CFTR mutations and IVS8-5T variant in newborns with hypertrypsinaemia and normal sweat test.
3. Increased Prevalence of Mutations of The Cystic Fibrosis Gene in Idiopathic Chronic and Recurrent Pancreatitis
4. Cystic Fibrosis Mutations in Heterozygous Newborns with Hypertrypsinemia and Low Sweat Chloride
5. Mutations in the Cystic Fibrosis Gene in Patients with Congenital Absence of the Vas Deferens
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