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: 2018/05/12 11:13
  • by administrador