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Nava C, Dalle C, Rastetter A, Striano P, de Kovel CG, Nabbout R, Canc├Ęs 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 (2014) De novo mutations in HCN1 cause early infantile epileptic encephalopathy. Nat Genet 46:640-5 [PubMed]

References and models cited by this paper

References and models that cite this paper

Miceli F, Soldovieri MV, Ambrosino P, De Maria M, Migliore M, Migliore R, Taglialatela M (2015) Early-onset epileptic encephalopathy caused by gain-of-function mutations in the voltage sensor of Kv7.2 and Kv7.3 potassium channel subunits. J Neurosci 35:3782-93 [Journal] [PubMed]
   Early-onset epileptic encephalopathy (Miceli et al. 2015) [Model]
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