Titel

Merkliste
1 Ergebnisse

De Novo Mutations in Synaptic Transmission Genes Including ..:

Appenzeller, Silke ; Balling, Rudi ; Barisic, Nina...
10.1016/j.ajhg.2014.08.013. , 2018

Link: http://hdl.handle.net/10138/231725

RT Journal
T1 <Title>De Novo Mutations in Synaptic Transmission Genes Including DNM1 Cause Epileptic Encephalopathies</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftunivhelsihelda:oai:helda.helsinki.fi:10138_231725&Exemplar=1&LAN=DE
				
A1 Appenzeller, Silke
A1 Balling, Rudi
A1 Barisic, Nina
A1 Baulac, Stephanie
A1 Caglayan, Hande
A1 Craiu, Dana
A1 De Jonghe, Peter
A1 Depienne, Christel
A1 Dimova, Petia
A1 Djemie, Tania
A1 Gormley, Padhraig
A1 Guerrini, Renzo
A1 Helbig, Ingo
A1 Hjalgrim, Helle
A1 Hoffman-Zacharska, Dorota
A1 Jaehn, Johanna
A1 Klein, Karl Martin
A1 Koeleman, Bobby
A1 Komarek, Vladimir
A1 Krause, Roland
A1 Kuhlenbaeumer, 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 Moller, 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 EuroEPINOMICS-RES Consortium
A1 Epilepsy Phenome Genome Project
A1 Epi4K Consortium
PB Cell Press
YR 2018
K1 INTELLECTUAL DISABILITY
K1 SPECTRUM DISORDERS
K1 GRIN2A MUTATIONS
K1 SCHIZOPHRENIA
K1 EPILEPSIES
K1 AUTISM
K1 ENDOCYTOSIS
K1 DYNAMIN-1
K1 PATTERNS
K1 APHASIA
K1 Neurosciences
JF 10.1016/j.ajhg.2014.08.013
LK http://hdl.handle.net/10138/231725
DO http://hdl.handle.net/10138/231725
SF ELIB - SuUB Bremen

Export

RefWorks (nur Desktop-Version!)
Flow (Zuerst in Flow einloggen, dann importieren)