Exome Sequencing and Rare Variant Analysis Reveals Multiple Filaggrin Mutations in Bangladeshi Families with Atopic Eczema and Additional Risk Genes
2018
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 grant
no. 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 research
and genetic orphan diseases
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