Carrier status for the common R501X and 2282del4 filaggrin mutations is not associated with hearing phenotypes in 5,377 children from the ALSPAC cohort.
PloS one 2009 4 (6): e5784.
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
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