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Novel SCN1A mutation in the IFMT motif of the α1 subunit of the voltage-gated NaV1.1 channel causing familial hemiplegic migraine

✍ Scribed by De Vries, B; Weller, CM; De Fàbregues, O; Koelewijn, SC; Stam, AH; Haan, J; Ferrari, MD; Terwindt, GM; van den Maagdenberg, AMJ


Book ID
121619635
Publisher
Springer
Year
2013
Tongue
English
Weight
54 KB
Volume
14
Category
Article
ISSN
1129-2369

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