Literature DB >> 16505326

SCN1A (2528delG) novel truncating mutation with benign outcome of severe myoclonic epilepsy of infancy.

S Buoni1, A Orrico, L Galli, R Zannolli, L Burroni, J Hayek, A Fois, V Sorrentino.   

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Year:  2006        PMID： 16505326     DOI： 10.1212/01.WNL.0000198504.41315.B1

Source DB:  PubMed          Journal:  Neurology        ISSN： 0028-3878            Impact factor:   9.910


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  1 in total

1.  Genetic background modulates impaired excitability of inhibitory neurons in a mouse model of Dravet syndrome.

Authors:  Moran Rubinstein; Ruth E Westenbroek; Frank H Yu; Christina J Jones; Todd Scheuer; William A Catterall
Journal:  Neurobiol Dis       Date:  2014-10-02       Impact factor: 5.996
  1 in total

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