Paroxysmal kinesigenic dyskinesia and myotonia congenita in the same family: coexistence of a PRRT2 mutation and two CLCN1 mutations
Crossref DOI link: https://doi.org/10.1007/s12264-014-1467-7
Published Online: 2014-09-05
Published Print: 2014-12
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Li, Hong-Fu
Chen, Wan-Jin
Ni, Wang
Wu, Zhi-Ying
Text and Data Mining valid from 2014-09-05