Filaggrin gene defects are associated with eczema, wheeze and nasal disease during infancy: prospective study : Sussex Research Online

Tools

Basu, Kaninika, Inglis, Sarah K, Bremner, Stephen A, Ramsay, Rebecca, Abd, Ali, Rabe, Heike, Strange, Elizabeth, Phillips, Veronica, Seddon, Paul, Tavendale, Roger, Memon, Anjum, Palmer, Colin N A, Fidler, Katy and Mukhopadhyay, Somnath (2020) Filaggrin gene defects are associated with eczema, wheeze and nasal disease during infancy: prospective study. Journal of Allergy and Clinical Immunology, 146 (3). pp. 681-682. ISSN 0091-6749

PDF - Accepted Version
Available under License Creative Commons Attribution-NonCommercial No Derivatives.
Download (902kB)

Official URL: https://doi.org/10.1016/j.jaci.2020.02.036

Abstract

This prospective cohort study describes associations between the presence of filaggrin gene mutations and eczema, rhinitis and wheeze from as early as age six months, raising new questions regarding underlying mechanisms and timing of interventions.

Item Type:	Article
Schools and Departments:	Brighton and Sussex Medical School > Clinical and Experimental Medicine Brighton and Sussex Medical School > Primary Care and Public Health
Subjects:	R Medicine > RJ Pediatrics > RJ0047.3 Genetic aspects
Depositing User:	Katie Isaac
Date Deposited:	11 Mar 2020 08:47
Last Modified:	28 Apr 2021 01:00
URI:	http://sro.sussex.ac.uk/id/eprint/90286

View download statistics for this item

📧 Request an update