Published January 1, 2016
| Version v1
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Pitfalls in genetic testing: the story of missed SCN1A mutations
Creators
- Djemie, Tania
- Weckhuysen, Sarah
- von Spiczak, Sarah1
- Carvill, Gemma L.2
- Jaehn, Johanna1
- Anttonen, Anna-Kaisa
- Brilstra, Eva3
- Caglayan, Hande S.4
- de Kovel, Carolien G.5
- Depienne, Christel
- Gaily, Eija6
- Hamalainen, Eija7
- Giraldez, Beatriz G.
- Gormley, Padhraig
- Guerrero-Lopez, Rosa
- Guerrini, Renzo8
- Hamalainen, Eija
- Hartmann, Corinna1
- Hernandez-Hernandez, Laura
- Hjalgrim, Helle
- Hjalgrim, Helle
- 1. Univ Med Ctr Schleswig Holstein, Dept Neuropediat, Kiel, Germany
- 2. Univ Washington, Dept Pediat, Div Med Genet, Seattle, WA 98195 USA
- 3. VIB, Dept Mol Genet, Neurogenet Grp, Antwerp, Belgium
- 4. Bogazici Univ, Dept Mol Biol & Genet, Istanbul, Turkey
- 5. Univ Med Ctr Utrecht, Dept Med Genet, Utrecht, Netherlands
- 6. Helsinki Univ Hosp, Dept Pediat Neurol, Helsinki, Finland
- 7. EO Osped Galliera, Genet Lab, Genoa, Italy
- 8. Univ Florence, A Meyer Childrens Hosp, Pediat Neurol & Neurogenet Unit & Labs, Florence, Italy
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