Population variation of common cystic fibrosis mutations
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference38 articles.
1. Development of RNA-SSCP protocols for the identification and screening of CFTR mutations: Identification of two new mutations
2. Identification of four new mutations in the cystic fibrosis transmembrane conductance regulator gene: I148T, L1077P, Y1092X, 2183AA→G
3. A new missense mutation (R1283M) in exon 20 of the cystic fibrosis transmembrane conductance regulator gene
4. A nonsense mutation in exon 4 of the cystic fibrosis gene frequent among the population of the Reunion Island
5. Identification of a frameshift mutation (1609delCA) in exon 10 of the CFTR gene in seven Spanish cystic fibrosis patients
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