Document is current

Any future updates will be listed below

First de novo KCND3 mutation causes severe Kv4.3 channel dysfunction leading to early onset cerebellar ataxia, intellectual disability, oral apraxia and epilepsy

Crossref DOI link: https://doi.org/10.1186/s12881-015-0200-3

Published Online: 2015-07-21

Published Print: 2015-12

Update policy: https://doi.org/10.1007/springer_crossmark_policy

About CrossMark