ABHD11(redirected from WBSCR21)
ABHD11A gene on chromosome 19p13.12 that encodes a member of a large family of proteins defined by an alpha/beta hydrolase fold.
ABHD11 is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of a block of contiguous genes at 7q11.23.
Segen's Medical Dictionary. © 2012 Farlex, Inc. All rights reserved.