PubMed 22274833
Referenced in: none
Automatically associated channels: Kir6.2
Title: Homozygous CFTR mutation M348K in a boy with respiratory symptoms and failure to thrive. Disease-causing mutation or benign alteration?
Authors: Julia Hentschel, Gabriele Riesener, Heike Nelle, Manfred Stuhrmann, Anja Schöner, Olaf Sommerburg, Eva Fritzsching, Marcus A Mall, Ferdinand von Eggeling, Jochen G Mainz
Journal, date & volume: Eur. J. Pediatr., 2012 Jul , 171, 1039-46
PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/22274833
Abstract