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Pitfalls in genetic testing: the story of missed SCN1A muta..:
Djémié, Tania
;
Weckhuysen, Sarah
;
von Spiczak, Sarah
...
10.1002/mgg3.217. , 2017
Link:
http://hdl.handle.net/10138/174550
RT Journal T1
Pitfalls in genetic testing: the story of missed SCN1A mutations
UL https://suche.suub.uni-bremen.de/peid=base-ftunivhelsihelda:oai:helda.helsinki.fi:10138_174550&Exemplar=1&LAN=DE A1 Djémié, Tania A1 Weckhuysen, Sarah A1 von Spiczak, Sarah A1 Carvill, Gemma L A1 Jaehn, Johanna A1 Anttonen, Anna-Kaisa A1 Brilstra, Eva A1 Caglayan, Hande S A1 de Kovel, Carolien G A1 Depienne, Christel A1 Gaily, Eija A1 Gennaro, Elena A1 Giraldez, Beatriz G A1 Gormley, Padraigh A1 Guerrero-López, Rosa A1 Guerrini, Renzo A1 Hämäläinen, Eija A1 Hartmann, Corinna A1 Hernandez-Hernandez, Laura A1 Hjalgrim, Helle A1 Koeleman, Bobby P.C A1 Leguern, Eric A1 Lehesjoki, Anna-Elina A1 Lemke, Johannes R A1 Leu, Costin A1 Marini, Carla A1 McMahon, Jacinta M A1 Mei, Davide A1 Møller, Rikke S A1 Myers, Candace T A1 Nava, Caroline A1 Serratosa, José M A1 Sisodiya, Sanjay M A1 Stephani, Ulrich A1 Striano, Pasquale A1 van Kempen, Marjan J.A A1 Verbeek, Nienke E A1 Usluer, Sunay A1 Zara, Federico A1 Palotie, Aarno A1 Meffiord, Heather C A1 Scheffer, Ingrid E A1 De Jonghe, Peter A1 Helbig, Ingo A1 Suls, Arvid A1 EuroEPINOMICS-RES Dravet working group PB Wiley YR 2017 K1 Biomedicine K1 Neurosciences K1 Neurology and psychiatry JF 10.1002/mgg3.217 LK http://hdl.handle.net/10138/174550 DO http://hdl.handle.net/10138/174550 SF ELIB - SuUB Bremen
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