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Carrier Status for the Common R501X and 2282del4 Filaggrin Mutations Is Not Associated with Hearing Phenotypes in 5377 Children from the ALSPAC Cohort
Rodriguez, Santiago, Hall, Amanda J., Granell, Raquel, McLean, W. H. Irwin, Irvine, Alan D., Palmer, Colin N. A., Smith, George Davey, Henderson, John, Day, Ian N. M., Schrijver, IrisVolume:
4
Language:
english
Journal:
PLoS ONE
DOI:
10.1371/journal.pone.0005784
Date:
June, 2009
File:
PDF, 91 KB
english, 2009