Referenced in: HCN1

Automatically associated channels: HCN1

Title: De novo mutations in HCN1 cause early infantile epileptic encephalopathy.

Authors: Caroline Nava, Carine Dalle, Agnès Rastetter, Pasquale Striano, Carolien G F de Kovel, Rima Nabbout, Claude Cancès, Dorothee 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, , Thomas Haaf, Eric LeGuern, Christel Depienne

Journal, date & volume: Nat. Genet., 2014 Jun , 46, 640-5

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/24747641

Abstract