Article (Scientific journals)
De novo mutations in HCN1 cause early infantile epileptic encephalopathy
Nava, Caroline; Dalle, Carine; Rastetter, Agnès et al.
2014In Nature Genetics
Peer reviewed
 

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Research center :
Luxembourg Centre for Systems Biomedicine (LCSB): Experimental Neurobiology (Balling Group)
Disciplines :
Genetics & genetic processes
Author, co-author :
Nava, Caroline
Dalle, Carine
Rastetter, Agnès
Striano, Pasquale
de Kovel, Carolien G. F.
Nabbout, Rima
Cancès, Claude
Ville, Dorothée
Brilstra, Eva H.
Gobbi, Giuseppe
Raffo, Emmanuel
Bouteiller, Delphine
Marie, Yannick
Trouillard, Oriane
Robbiano, Angela
Keren, Boris
Agher, Dahbia
Roze, Emmanuel
Lesage, Suzanne
Nicolas, Aude
Brice, Alexis
Baulac, Michel
Vogt, Cornelia
El Hajj, Nady
Schneider, Eberhard
Suls, Arvid
Weckhuysen, Sarah
Gormley, Padhraig
Lehesjoki, Anna-Elina
De Jonghe, Peter
Helbig, Ingo
Baulac, Stephanie
Zara, Federico
Koeleman, Bobby P. C.
Consortium, Euroepinomics R. E. S.
Haaf, Thomas
LeGuern, Eric
Depienne, Christel
More authors (28 more) Less
Other collaborator :
May, Patrick  ;  University of Luxembourg > Luxembourg Centre for Systems Biomedicine (LCSB)
Balling, Rudi ;  University of Luxembourg > Luxembourg Centre for Systems Biomedicine (LCSB)
Barisic, Nina
Baulac, Stéphanie
Caglayan, Hande S.
Craiu, Dana C.
De Jonghe, Peter
Depienne, Christel
Gormley, Padhraig
Guerrini, Renzo
Helbig, Ingo
Hjalgrim, Helle
Hoffman-Zacharska, Dorota
Jähn, Johanna
Klein, Karl Martin
Koeleman, Bobby P. C.
Komarek, Vladimir
Krause, Roland  ;  University of Luxembourg > Luxembourg Centre for Systems Biomedicine (LCSB)
LeGuern, Eric
Lehesjoki, Anna-Elina
Lemke, Johannes R.
Lerche, Holger
Marini, Carla
Møller, Rikke S.
Muhle, Hiltrud
Palotie, Aarno
Pal, Deb
Rosenow, Felix
Selmer, Kaja
Serratosa, José M.
Sisodiya, Sanjay
Stephani, Ulrich
Sterbova, Katalin
Striano, Pasquale
Suls, Arvid
Talvik, Tiina
von Spiczak, Sarah
Weber, Yvonne
Weckhuysen, Sarah
Zara, Federico
More authors (30 more) Less
External co-authors :
yes
Language :
English
Title :
De novo mutations in HCN1 cause early infantile epileptic encephalopathy
Publication date :
20 April 2014
Journal title :
Nature Genetics
Publisher :
Nature Publishing Group
Peer reviewed :
Peer reviewed
Available on ORBilu :
since 29 April 2014

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