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Mutations in KCNT1 cause a spectrum of focal epilepsies
- Authors :
- Genetica Sectie Genoomdiagnostiek
Child Health
Brain
Møller, Rikke S.
Heron, Sarah E.
Larsen, Line H G
Lim, Chiao Xin
Ricos, Michael G.
Bayly, Marta A.
Van Kempen, Marjan J A
Klinkenberg, Sylvia
Andrews, Ian
Kelley, Kent
Ronen, Gabriel M.
Callen, David
McMahon, Jacinta M.
Yendle, Simone C.
Carvill, Gemma L.
Mefford, Heather C.
Nabbout, Rima
Poduri, Annapurna
Striano, Pasquale
Baglietto, Maria G.
Zara, Federico
Smith, Nicholas J.
Pridmore, Clair
Gardella, Elena
Nikanorova, Marina
Dahl, Hans Atli
Gellert, Pia
Scheffer, Ingrid E.
Gunning, Boudewijn
Kragh-Olsen, Bente
Dibbens, Leanne M.
Genetica Sectie Genoomdiagnostiek
Child Health
Brain
Møller, Rikke S.
Heron, Sarah E.
Larsen, Line H G
Lim, Chiao Xin
Ricos, Michael G.
Bayly, Marta A.
Van Kempen, Marjan J A
Klinkenberg, Sylvia
Andrews, Ian
Kelley, Kent
Ronen, Gabriel M.
Callen, David
McMahon, Jacinta M.
Yendle, Simone C.
Carvill, Gemma L.
Mefford, Heather C.
Nabbout, Rima
Poduri, Annapurna
Striano, Pasquale
Baglietto, Maria G.
Zara, Federico
Smith, Nicholas J.
Pridmore, Clair
Gardella, Elena
Nikanorova, Marina
Dahl, Hans Atli
Gellert, Pia
Scheffer, Ingrid E.
Gunning, Boudewijn
Kragh-Olsen, Bente
Dibbens, Leanne M.
- Publication Year :
- 2015
Details
- Database :
- OAIster
- Notes :
- English
- Publication Type :
- Electronic Resource
- Accession number :
- edsoai.on1395273266
- Document Type :
- Electronic Resource