Exome sequencing and rare variant analysis reveals multiple filaggrin mutations in Bangladeshi atopic eczema families and additional risk genes.

M.P was supported by a Fellowship from the German Research Foundation (DFG).This work received infrastructure support through the DFG Cluster of Excellence“Inflammation at Interfaces” (grants EXC306 and EXC306/2), and was supported by grants(WE2678/6-1, WE2678/6-2, WE2678/9) from the DFG and the e:Med sysINFLAME grantno. 01ZX1306A from the German Federal Ministry of Education and Research (BMBF).J.E.A.C. and X.F.C.C.W. are funded by A*STAR SPF funding for translational skin researchand genetic orphan diseases