Carrier Status for the Common R501X and 2282del4 Filaggrin Mutations Is Not Associated with Hearing Phenotypes in 5377 Children from the ALSPAC Cohort

S Rodríguez, AJ Hall, R Granell, Irwin WH McClean, AD Irvine, CNA Palmer, G Davey Smith, J Henderson, INM Day

Research output: Contribution to journalArticle (Academic Journal)peer-review

5 Citations (Scopus)
Translated title of the contributionCarrier Status for the Common R501X and 2282del4 Filaggrin Mutations Is Not Associated with Hearing Phenotypes in 5377 Children from the ALSPAC Cohort
Original languageEnglish
Pages (from-to)e5784
JournalPLoS ONE
Volume4
Issue number6
DOIs
Publication statusPublished - Jun 2009

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