Show pageBacklinksCite current pageExport to PDFBack to top This page is read only. You can view the source, but not change it. Ask your administrator if you think this is wrong. [[GFAP]] is a type III [[intermediate filament]] (IF) protein that maps, in humans, to [[17q21]]. 7q21.31 [[microdeletion syndrome]], also known as Koolen–de Vries syndrome (KdVS), is a rare genetic disorder caused by a deletion of a segment of chromosome 17 which contains six genes. This deletion syndrome was discovered independently in 2006 by three different research groups. 17q21.txt Last modified: 2024/06/07 02:56by 127.0.0.1