De novo in-frame deletions and duplications in the SPTAN1 gene, encoding the non-erythrocyte aII spectrin, have been associated with severe West syndrome with hypomyelination and pontocerebellar atrophy. We aimed at comprehensively delineating the phenotypic spectrum associated with SPTAN1 mutations.

Delineating SPTAN1 associated phenotypes : from isolated epilepsy to encephalopathy with progressive brain atrophy / Syrbe, S; L, Harms F.; Parrini, E; Montomoli, M; Mu Tze, U; L, Heldig K.; Polster, T; Albrecht, B; Bernbeck, U; Van Binsbergen, E; Biskup, S; Burglen, L; Denecke, J; Heron, B; Heyne H, O.; F, Hoffman G.; Hornemann, F; Matsushige, T; Matsuura, R; Kato, M; C, Korenke G.; Kuechler, A; La mmer, C; Merkenschager, A; Mignot, C; Ruf, S; Nakashima, M; Saitsu, H; Stamberger, H; Pisano, T; Tohyama, J; Weckhuysen, S; Werckx, W; Wickert, J; Mari, F; E, Verbeek N.; S, Moller R.; Koeleman, B; Matsumoto, N; B, Dobyns W.; Battaglia, D; R, Lemke J.; Kutsche, K; Guerrini, R.. - In: BRAIN. - ISSN 0006-8950. - ELETTRONICO. - (2017), pp. 2322-2336.

Delineating SPTAN1 associated phenotypes : from isolated epilepsy to encephalopathy with progressive brain atrophy

Parrini E;MONTOMOLI, MARTINO;Guerrini R.
2017

Abstract

De novo in-frame deletions and duplications in the SPTAN1 gene, encoding the non-erythrocyte aII spectrin, have been associated with severe West syndrome with hypomyelination and pontocerebellar atrophy. We aimed at comprehensively delineating the phenotypic spectrum associated with SPTAN1 mutations.
2017
2322
2336
Syrbe, S; L, Harms F.; Parrini, E; Montomoli, M; Mu Tze, U; L, Heldig K.; Polster, T; Albrecht, B; Bernbeck, U; Van Binsbergen, E; Biskup, S; Burglen,...espandi
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/1108916
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