Exome sequencing identifies a rare HSPG2 variant associated with familial idiopathic scoliosis. - Baschal EE; Wethey CI; Swindle K; Baschal RM; Gowan K; Tang NL; Alvarado DM; Haller GE; Dobbs MB; Taylor MR; Gurnett CA; Jones KL; et al. (G3 (Bethesda, Md.), 2014)