| Title | Novel mutations in HINT1 gene cause autosomal recessive axonal neuropathy with neuromyotonia in Chinese patients. |
| Authors | Meng, Lingchao Fu, Jun Lv, He Zhang, Wei Wang, Zhaoxia Yuan, Yun |
| Affiliation | Peking Univ, Hosp 1, Beijing, Peoples R China. |
| Keywords | CMTR PHENOTYPE DISEASE |
| Issue Date | 2018 |
| Publisher | JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM |
| Citation | JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM. 2018, 23(4), 345-345. |
| URI | http://hdl.handle.net/20.500.11897/571298 |
| ISSN | 1085-9489 |
| Indexed | SCI(E) |
| Appears in Collections: | 第一医院 |
