Publication
De novo mutations in HCN1 cause early infantile epileptic encephalopathy
Caroline Nava, Carine Dalle, Agnès Rastetter, Pasquale Striano, Carolien G F de Kovel, Rima Nabbout, Claude Cancès, Dorothée Ville, Eva H Brilstra, Giuseppe Gobbi, Emmanuel Raffo, Delphine Bouteiller, Yannick Marie, Oriane Trouillard, Angela Robbiano, Boris Keren, Dahbia Agher, Emmanuel Roze, Suzanne Lesage, Aude Nicolas, Alexis Brice, Michel Baulac, Cornelia Vogt, Nady El Hajj, Eberhard Schneider, Arvid Suls, Sarah Weckhuysen, Padhraig Gormley, Anna-Elina Lehesjoki, Peter De Jonghe, Ingo Helbig, Stéphanie Baulac, Federico Zara, Bobby P C Koeleman, Rudi Balling, Nina Barisic, Stéphanie Baulac, Hande S Caglayan, Dana C Craiu, Peter De Jonghe, Christel Depienne, Padhraig Gormley, Renzo Guerrini, Ingo Helbig, Helle Hjalgrim, Dorota Hoffman-Zacharska, Johanna Jähn, Karl Martin Klein, Bobby P C Koeleman, Vladimir Komarek, Roland Krause, Eric LeGuern, Anna-Elina Lehesjoki, Johannes R Lemke, Holger Lerche, Carla Marini, Patrick May, Rikke S Møller, Hiltrud Muhle, Aarno Palotie, Deb Pal, Felix Rosenow, Kaja Selmer, José M Serratosa, Sanjay Sisodiya, Ulrich Stephani, Katalin Sterbova, Pasquale Striano, Arvid Suls, Tiina Talvik, Sarah von Spiczak, Yvonne Weber, Sarah Weckhuysen, Federico Zara, Thomas Haaf, Eric LeGuern, Christel Depienne
Nature Genetics, April 2014, Nature
DOI: 10.1038/ng.2952