Report on the p.Ser489X (p.Ser489*) CFTR mutation, a...

Genetics in Medicine 2012 / 10 Vol. 14; Iss. 10

Report on the p.Ser489X (p.Ser489*) CFTR mutation, a variant with severe associated phenotype and high prevalence in a Quebec French-Canadian cystic fibrosis patient population

De Bie, Isabelle, Agatep, Ron, Scott, Patrick, Ruchon, Andrea
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Volume:
14
Language:
english
Journal:
Genetics in Medicine
DOI:
10.1038/gim.2012.57
Date:
October, 2012
File:
PDF, 215 KB
english, 2012
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