1. Identification of novel mutation in RANKL by whole‐exome sequencing in a Thai family with osteopetrosis; a case report and review of RANKL osteopetrosis. Issue 7 (30th May 2021) Authors: Lertwilaiwittaya, Pongtawat; Suktitipat, Bhoom; Khongthon, Phongphak; Pongsapich, Warut; Limwongse, Chanin; Pithukpakorn, Manop Journal: Molecular genetics & genomic medicine Issue: Volume 9:Issue 7(2021) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗