Carrier status for the common R501X and 2282del4 filaggrin mutations is not associated with hearing phenotypes in 5,377 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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Medicine & Life Sciences