Referenced in: none

Automatically associated channels: Kir2.3 , Kir6.2 , Kv2.1

Title: Cystic fibrosis patients bearing both the common missense mutation Gly----Asp at codon 551 and the delta F508 mutation are clinically indistinguishable from delta F508 homozygotes, except for decreased risk of meconium ileus.

Authors: A Hamosh, T M King, B J Rosenstein, M Corey, H Levison, P Durie, L C Tsui, I McIntosh, M Keston, D J Brock

Journal, date & volume: Am. J. Hum. Genet., 1992 Aug , 51, 245-50

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/1379413

Abstract