Recurrent and novel mutations in the NTRK1 gene lead to rare congenital insensitivity to pain with anhidrosis in two Chinese patients

Fang Lv(Liaoning Normal University), Mei Li(Yantaishan Hospital), Weibo Xia(Chinese Academy of Medical Sciences & Peking Union Medical College), Lujiao Li(Chinese Academy of Medical Sciences & Peking Union Medical College), Yan Jiang(Chinese Academy of Medical Sciences & Peking Union Medical College), Peng Gao(Chinese Academy of Medical Sciences & Peking Union Medical College), Yuwen Song(Chinese Academy of Medical Sciences & Peking Union Medical College), Ou Wang(Chinese Academy of Medical Sciences & Peking Union Medical College), Xiaojie Xu(Dalian Medical University), Xiaoping Xing(Chinese Academy of Medical Sciences & Peking Union Medical College)
Clinica Chimica Acta
February 10, 2017
10.1016/j.cca.2017.02.007
Cited by 22

Related Papers

Neoadjuvant PD-1 inhibitor (Sintilimab) in NSCLC
|Journal of Thoracic Oncology|2020|415
Luteolin-loaded solid lipid nanoparticles synthesis, characterization, & improvement of bioavailability, pharmacokinetics in vitro and vivo studies
|Journal of Nanoparticle Research|2014|128
CircCEMIP promotes anoikis-resistance by enhancing protective autophagy in prostate cancer cells
|Journal of Experimental & Clinical Cancer Research|2022|115
Denosumab or romosozumab therapy and risk of cardiovascular events in patients with primary osteoporosis: Systematic review and meta- analysis
|Bone|2019|110
The influence of different growth hormone addition protocols to poor ovarian responders on clinical outcomes in controlled ovary stimulation cycles
|Medicine|2017|100