| Home | E-Submission | Sitemap | Editorial Office |  
top_img
 ACN Search

A novel p.Leu699Pro mutation in MFN2 gene causes Charcot-Marie-Tooth disease type 2A
Sa-Yoon Kang, Keun Hyuk Ko, Jung-Hwan Oh
Ann Clin Neurophysiol. 2019; 21(1): 57-60.   Published online January 29, 2019
doi: https://doi.org/10.14253/acn.2019.21.1.57
  PDF Links       
 
Diagnosis and treatment in Charcot-Marie-Tooth disease
Sang-Beom Kim, Kee-Duk Park, Byung-Ok Choi
Korean J Clin Neurophysiol. 2005; 7(2): 65-74.
  PDF Links       
 
Clinical and Electrophysiological Features of HNPP Patients with 17p11.2 Deletion
Yoon-Ho Hong, Manho Kim, Jung-Joon Sung, Sung Hun Kim, Kwang-Woo Lee
Korean J Clin Neurophysiol. 2002; 4(2): 125-132.
  PDF Links       
 
1 |
E-Submission
Email Alert
Endnote Style Download
Author's Index
Korean Society of Phycology
KoreaMed
KoMCI
GoogleScholar
Similarity Check
KOFST
COPE
MeSH on Demand
ORCID
Editorial Office
Department of Neurology, Seoul National University (SNU) College of Medicine
SMG-SNU Boramae Medical Center
20 Boramaero-5-Gil, Dongjak-Gu, Seoul 07061, Republic of Korea
TEL : +82-2-2266-7238    FAX : +82-2-831-2826   E-mail: acn.journal@e-acn.org
About |  Browse Articles |  Current Issue |  For Authors and Reviewers
Copyright © The Korean Society of Clinical Neurophysiology.           Developed in M2PI