Intronic PRRT2 mutation generates novel splice acceptor site and causes paroxysmal kinesigenic dyskinesia with infantile convulsions (PKD/IC) in a three generation family
Crossref DOI link: https://doi.org/10.1186/s12881-016-0281-7
Published Online: 2016-03-03
Published Print: 2016-12
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Weber, Axel
Kreth, Jonas
Müller, Ulrich