Djémié, Tania ;
Weckhuysen, Sarah ;
von Spiczak, Sarah...
Djémié , T , Weckhuysen , S , von Spiczak , S , Carvill , G L , Jaehn , J , Anttonen , A-K , Brilstra , E , Caglayan , H S , de Kovel , C G , Depienne , C , Gaily , E , Gennaro , E , Giraldez , B G , Gormley , P , Guerrero-López , R , Guerrini , R , Hämäläinen , E , Hartmann , C , Hernandez-Hernandez , L , Hjalgrim , H , Koeleman , B P C , Leguern , E , Lehesjoki , A-E , Lemke , J R , Leu , C , Marini , C , McMahon , J M , Mei , D , Møller , R S , Muhle , H , Myers , C T , Nava , C , Serratosa , J M , Sisodiya , S M , Stephani , U , Striano , P , van Kempen , M J A , Verbeek , N E , Usluer , S , Zara , F , Palotie , A , Mefford , H C , Scheffer , I E , De Jonghe , P , Helbig , I , Suls , A & EuroEPINOMICS‐RES Dravet working group 2016 , ' Pitfalls in genetic testing : the story of missed SCN1A mutations ' , Molecular Genetics & Genomic Medicine , vol. 4 , no. 4 , pp. 457-464 . https://doi.org/10.1002/mgg3.217.
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2016
