De novo SCN1A mutations in Dravet syndrome and related epileptic encephalopathies are largely of paternal origin (Q57905641)
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scientific article published on 08 July 2009
Language | Label | Description | Also known as |
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English | De novo SCN1A mutations in Dravet syndrome and related epileptic encephalopathies are largely of paternal origin |
scientific article published on 08 July 2009 |
Statements
De novo SCN1A mutations in Dravet syndrome and related epileptic encephalopathies are largely of paternal origin (English)
Xenia Iona
Sameer M Zuberi
Rachael Birch
Carla M Bruce