TY - JOUR AU - Wu, Xing AU - Chen, Lanlan AU - Zhang, Yixin AU - Xie, Hainan AU - Xue, Meirong AU - Wang, Yi AU - Huang, Houbin PY - 2018 DA - 2018/11/26 TI - A novel mutation in the VHL gene in a Chinese family with von Hippel-Lindau disease JO - BMC Medical Genetics SP - 204 VL - 19 IS - 1 AB - Von Hippel-Lindau (VHL) disease is an autosomal dominant inherited cancer syndrome, and VHL is identified as a tumor suppressor gene. The main objective of this study was to identify disease-causing mutations in a Chinese family affected with VHL disease. SN - 1471-2350 UR - https://doi.org/10.1186/s12881-018-0716-4 DO - 10.1186/s12881-018-0716-4 ID - Wu2018 ER -