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Pitfalls in genetic testing : the story of missed SCN1A mut..:
Djémié, Tania
;
Weckhuysen, Sarah
;
von Spiczak, Sarah
...
2324-9269. , 2016
Link:
https://dspace.library.uu.nl/handle/1874/336898
RT Journal T1
Pitfalls in genetic testing : the story of missed SCN1A mutations
UL https://suche.suub.uni-bremen.de/peid=base-ftunivutrecht:oai:dspace.library.uu.nl:1874_336898&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, Padhraig 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 Muhle, Hiltrud A1 Myers, Candace T A1 Nava, Caroline A1 Serratosa, Jose 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 Mefford, Heather C A1 Scheffer, Ingrid E A1 De Jonghe, Peter A1 Helbig, Ingo A1 Suls, Arvid A1 EuroEPINOMICS‐RES Dravet working group YR 2016 K1 Dravet syndrome K1 epilepsy K1 genetic screening K1 next-generation sequencing K1 Sanger sequencing K1 Journal Article JF 2324-9269 LK http://dx.doi.org/https://dspace.library.uu.nl/handle/1874/336898 DO https://dspace.library.uu.nl/handle/1874/336898 SF ELIB - SuUB Bremen
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