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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