Aberrant signature methylome by DNMT1 hot spot mutation in hereditary sensory and autonomic neuropathy 1E
Zhifu Sun(Mayo Clinic), Christopher J. Klein(Mayo Clinic), Kaori Hojo, Tamás Ördög(Mayo Clinic), Yanhong Wu(Shandong University of Technology), Jean-Pierre Kocher(Mayo Clinic), Jinfu Nie(Hefei Institutes of Physical Science), Xiaohui Duan(Shandong University), Saurabh Baheti(Mayo Clinic in Florida), P. James B. Dyck(Mayo Clinic)
Cited by 64
Related Papers
Patisiran, an RNAi Therapeutic, for Hereditary Transthyretin Amyloidosis
|New England Journal of Medicine|2018|2.9k
Inotersen Treatment for Patients with Hereditary Transthyretin Amyloidosis
|New England Journal of Medicine|2018|1.4k
Autoimmune encephalitis epidemiology and a comparison to infectious encephalitis
|Annals of Neurology|2018|758