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17q21

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