SCN1A gene sequencing in 46 Turkish epilepsy patients disclosed 12 novel mutations-Reference-Cited by-同舟云学术

SCN1A gene sequencing in 46 Turkish epilepsy patients disclosed 12 novel mutations

Published:2016-07 Issue: Volume:39 Page:34-43
ISSN:1059-1311
Container-title:Seizure
language:en
Short-container-title:Seizure

Author:

Usluer Sunay,Salar Seda,Arslan Mutluay,Yiş Uluç,Kara Bülent,Tektürk Pınar,Baykan Betül,Meral Cihan,Türkdoğan Dilşad,Bebek Nerses,Yalçın Çapan Özlem,Gündoğdu Eken Aslı,Çağlayan S. Hande

Publisher

Elsevier BV

Subject

Neurology (clinical),Neurology,General Medicine

Reference33 articles.

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2. De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy;Claes;Am J Hum Genet,2001

3. A novel SCN1A mutation associated with generalized epilepsy with febrile seizures plus--and prevalence of variants in patients with epilepsy;Escayg;Am J Hum Genet,2001

4. The spectrum of SCN1A-related infantile epileptic encephalopathies;Harkin;Brain,2007

5. Balanced translocation in a patient with severe myoclonic epilepsy of infancy disrupts the sodium channel gene SCN1A;Møller;Epilepsia,2008

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