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1 research outputs found
Clinical exome sequencing identifies two novel mutations of the SCN1A and SCN2A genes in Moroccan patients with epilepsy: a case series
Author
Abdelali Zrhidri
Abdelaziz Sefiani
+19Â more
AS Allen
B Tumiene
BL Fogel
CT Myers
Fatima Zohra Oudghiri
H Kodera
Jaber Lyahyai
KM Fiest
Maryem Sahli
MM Mancardi
NM Allen
NS Santhosh
RS Fisher
S Liu
S Usluer
Sara Matricardi
Siham Chafai Elaloui
Wiam Smaili
Y Xue
Publication venue
'Springer Science and Business Media LLC'
Publication date
Field of study
No full text
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