De novo mutations in HCN1 cause early infantile epileptic encephalopathy.
De novo mutations in HCN1 cause early infantile epileptic encephalopathy / Nava C; Dalle C; Rastetter A; Striano P; de Kovel CG; Nabbout R; Cancès C; Ville D; Brilstra EH; Gobbi G; Raffo E; Bouteiller D; Marie Y; Trouillard O; Robbiano A; Keren B; Agher D; Roze E; Lesage S; Nicolas A; Brice A; Baulac M; Vogt C; El Hajj N; Schneider E; Suls A; Weckhuysen S; Gormley P; Lehesjoki AE; De Jonghe P; Helbig I; Baulac S; Zara F; Koeleman BP; EuroEPINOMICS RES Consortium; Haaf T; LeGuern E; Depienne C. Collaborators: Balling R; Barisic N; Baulac S; Caglayan HS; Craiu DC; De Jonghe P; Depienne C; Gormley P; Guerrini R; Helbig I; Hjalgrim H; Hoffman-Zacharska D; Jähn J; Klein KM; Koeleman BP; Komarek V; Krause R; LeGuern E; Lehesjoki AE; Lemke JR; Lerche H; Marini C; May P; Møller RS; Muhle H;Palotie A; Pal D; Rosenow F; Selmer K; Serratosa JM; Sisodiya S; Stephani U; Sterbova K; Striano P; Suls A; Talvik T; von Spiczak S; Weber Y;Weckhuysen S; Zara F.. - In: NATURE GENETICS. - ISSN 1061-4036. - STAMPA. - 46 (6):(2014), pp. 640-645.
De novo mutations in HCN1 cause early infantile epileptic encephalopathy.
GUERRINI, RENZO;Marini C;
2014
Abstract
De novo mutations in HCN1 cause early infantile epileptic encephalopathy.
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