Exome Sequencing and Rare Variant Analysis Reveals Multiple Filaggrin Mutations in Bangladeshi Families with Atopic Eczema and Additional Risk Genes

Manuela Pigors, John E. A. Common, Xuan Fei Colin C. Wong, Sajid Malik, Claire A. Scott, Niloofar Tabarra, Herty Liany, Jianjun Liu, Vachiranee Limviphuvadh, Sebastian Maurer-Stroh, Mark By Tang, Nicholas Lench, David J. Margolis, David A. van Heel, Charles A. Mein, Natalija Novak, Hansjörg Baurecht, Stephan Weidinger, W. H. Irwin McLean, Alan D. IrvineEdel A. O'Toole, Michael A. Simpson, David P. Kelsell

Research output: Contribution to journalLetter

13 Citations (Scopus)
99 Downloads (Pure)
Original languageEnglish
Pages (from-to)2674-2677
Number of pages4
JournalJournal of Investigative Dermatology
Volume138
Issue number12
Early online date30 May 2018
DOIs
Publication statusPublished - Dec 2018

Cite this

Pigors, M., Common, J. E. A., Wong, X. F. C. C., Malik, S., Scott, C. A., Tabarra, N., Liany, H., Liu, J., Limviphuvadh, V., Maurer-Stroh, S., Tang, M. B., Lench, N., Margolis, D. J., van Heel, D. A., Mein, C. A., Novak, N., Baurecht, H., Weidinger, S., McLean, W. H. I., ... Kelsell, D. P. (2018). Exome Sequencing and Rare Variant Analysis Reveals Multiple Filaggrin Mutations in Bangladeshi Families with Atopic Eczema and Additional Risk Genes. Journal of Investigative Dermatology, 138(12), 2674-2677. https://doi.org/10.1016/j.jid.2018.05.013