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1 Ergebnisse
1
De Novo Mutations in Synaptic Transmission Genes Including ..:
Appenzeller, Silke
;
Balling, Rudi
;
Barisic, Nina
...
qt4805b6c0. , 2014
Link:
https://escholarship.org/uc/item/4805b6c0
RT Journal T1
De Novo Mutations in Synaptic Transmission Genes Including DNM1 Cause Epileptic Encephalopathies
UL https://suche.suub.uni-bremen.de/peid=base-ftcdlib:oai:escholarship.org:ark:_13030_qt4805b6c0&Exemplar=1&LAN=DE A1 Appenzeller, Silke A1 Balling, Rudi A1 Barisic, Nina A1 Baulac, Stéphanie A1 Caglayan, Hande A1 Craiu, Dana A1 De Jonghe, Peter A1 Depienne, Christel A1 Dimova, Petia A1 Djémié, Tania A1 Gormley, Padhraig A1 Guerrini, Renzo A1 Helbig, Ingo A1 Hjalgrim, Helle A1 Hoffman-Zacharska, Dorota A1 Jähn, Johanna A1 Klein, Karl Martin A1 Koeleman, Bobby A1 Komarek, Vladimir A1 Krause, Roland A1 Kuhlenbäumer, Gregor A1 Leguern, Eric A1 Lehesjoki, Anna-Elina A1 Lemke, Johannes R A1 Lerche, Holger A1 Linnankivi, Tarja A1 Marini, Carla A1 May, Patrick A1 Møller, Rikke S A1 Muhle, Hiltrud A1 Pal, Deb A1 Palotie, Aarno A1 Pendziwiat, Manuela A1 Robbiano, Angela A1 Roelens, Filip A1 Rosenow, Felix A1 Selmer, Kaja A1 Serratosa, Jose M A1 Sisodiya, Sanjay A1 Stephani, Ulrich A1 Sterbova, Katalin A1 Striano, Pasquale A1 Suls, Arvid A1 Talvik, Tiina A1 von Spiczak, Sarah A1 Weber, Yvonne A1 Weckhuysen, Sarah A1 Zara, Federico A1 Abou-Khalil, Bassel A1 Alldredge, Brian K A1 Andermann, Eva A1 Andermann, Frederick A1 Amron, Dina A1 Bautista, Jocelyn F A1 Berkovic, Samuel F A1 Bluvstein, Judith A1 Boro, Alex A1 Cascino, Gregory A1 Consalvo, Damian A1 Crumrine, Patricia A1 Devinsky, Orrin A1 Dlugos, Dennis A1 Epstein, Michael P A1 Fiol, Miguel A1 Fountain, Nathan B A1 French, Jacqueline A1 Friedman, Daniel A1 Geller, Eric B A1 Glauser, Tracy A1 Glynn, Simon A1 Haas, Kevin A1 Haut, Sheryl R A1 Hayward, Jean A1 Helmers, Sandra L A1 Joshi, Sucheta A1 Kanner, Andres A1 Kirsch, Heidi E A1 Knowlton, Robert C A1 Kossoff, Eric H A1 Kuperman, Rachel A1 Kuzniecky, Ruben A1 Lowenstein, Daniel H A1 McGuire, Shannon M A1 Motika, Paul V A1 Novotny, Edward J A1 Ottman, Ruth A1 Paolicchi, Juliann M A1 Parent, Jack A1 Park, Kristen A1 Poduri, Annapurna A1 Sadleir, Lynette A1 Scheffer, Ingrid E A1 Shellhaas, Renée A A1 Sherr, Elliott A1 Shih, Jerry J A1 Singh, Rani A1 Sirven, Joseph A1 Smith, Michael C A1 Sullivan, Joe A1 Thio, Liu Lin PB eScholarship, University of California YR 2014 K1 Genetics K1 Pediatric K1 Neurosciences K1 Epilepsy K1 Brain Disorders K1 Neurodegenerative K1 2.1 Biological and endogenous factors K1 Aetiology K1 Cohort Studies K1 Dynamin I K1 Exome K1 Fatty Acid Synthase K1 Type I K1 Female K1 Gene Regulatory Networks K1 Humans K1 Infant K1 Newborn K1 Lennox Gastaut Syndrome K1 Male K1 Mutation K1 Protein Interaction Maps K1 Receptors K1 GABA-B K1 Ryanodine Receptor Calcium Release Channel K1 Spasms K1 Infantile K1 Synaptic Transmission K1 EuroEPINOMICS-RES Consortium K1 Epilepsy Phenome/Genome Project K1 Epi4K Consortium K1 Biological Sciences K1 Medical and Health Sciences K1 Genetics & Heredity JF qt4805b6c0 LK http://dx.doi.org/https://escholarship.org/uc/item/4805b6c0 DO https://escholarship.org/uc/item/4805b6c0 SF ELIB - SuUB Bremen
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