First de novo KCND3 mutation causes severe Kv4.3 channel dysfunction leading to early onset cerebellar ataxia, intellectual disability, oral apraxia and epilepsy (Q35696704)
Jump to navigation
Jump to search
scientific article published on 21 July 2015
Language | Label | Description | Also known as |
---|---|---|---|
English | First de novo KCND3 mutation causes severe Kv4.3 channel dysfunction leading to early onset cerebellar ataxia, intellectual disability, oral apraxia and epilepsy |
scientific article published on 21 July 2015 |
Statements
1 reference
First de novo KCND3 mutation causes severe Kv4.3 channel dysfunction leading to early onset cerebellar ataxia, intellectual disability, oral apraxia and epilepsy (English)
1 reference
Rebecca Schüle
1 reference
Stephan Züchner
1 reference
Katrien Smets
1 reference
Anna Duarri
1 reference
Tine Deconinck
1 reference
Berten Ceulemans
1 reference
Bart P van de Warrenburg
1 reference
Michael Anthony Gonzalez
1 reference
Nathalie Van der Aa
1 reference
Peter De Jonghe
1 reference
Dineke S Verbeek
1 reference
Jonathan Baets
1 reference
21 July 2015
1 reference
1 reference
16
1 reference
51
1 reference
21 July 2015
1 reference
Identifiers
1 reference
1 reference
1 reference