Carrier status for the common R501X and 2282del4 filaggrin mutations is not associated with hearing phenotypes in 5377 children from the ALSPAC cohort
Santiago Rodriguez, Amanda J. Hall, Raquel Granell, W. H. Irwin McLean, Alan D. Irvine, Colin N. A. Palmer, George Davey Smith, John Henderson, Ian N. M. Day
Research output: Contribution to journal › Article › peer-review
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