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Mutations in the CLCN2 gene are a rare cause of idiopathic generalized epilepsy syndromes. [electronic resource] by
- Stogmann, E
- Lichtner, P
- Baumgartner, C
- Schmied, M
- Hotzy, C
- Asmus, F
- Leutmezer, F
- Bonelli, S
- Assem-Hilger, E
- Vass, K
- Hatala, K
- Strom, T M
- Meitinger, T
- Zimprich, F
- Zimprich, A
Producer: 20070912
In:
Neurogenetics vol. 7
Availability: No items available.
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A novel homozygous change of [electronic resource] by
- Giorgio, Elisa
- Vaula, Giovanna
- Benna, Paolo
- Lo Buono, Nicola
- Eandi, Chiara Maria
- Dino, Daniele
- Mancini, Cecilia
- Cavalieri, Simona
- Di Gregorio, Eleonora
- Pozzi, Elisa
- Ferrero, Marta
- Giordana, Maria Teresa
- Depienne, Christel
- Brusco, Alfredo
Producer: 20190204
In:
Journal of neurology, neurosurgery, and psychiatry vol. 88
Availability: No items available.
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Impaired surface membrane insertion of homo- and heterodimeric human muscle chloride channels carrying amino-terminal myotonia-causing mutations. [electronic resource] by
- Ronstedt, Katharina
- Sternberg, Damien
- Detro-Dassen, Silvia
- Gramkow, Thomas
- Begemann, Birgit
- Becher, Toni
- Kilian, Petra
- Grieschat, Matthias
- Machtens, Jan-Philipp
- Schmalzing, Günther
- Fischer, Martin
- Fahlke, Christoph
Producer: 20160919
In:
Scientific reports vol. 5
Availability: No items available.
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