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Academic Journal

A Functional Null Mutation of SCN1B in a Patient with Dravet Syndrome.

Subjects: EPILEPSY; INFANT diseases; SODIUM channels

  • Source: Journal of Neuroscience; 8/26/2009, Vol. 29 Issue 34, p10764-10778, 15p, 4 Diagrams, 6 Charts, 4 Graphs

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  • 1-5 of  5 results for ""SANTIAGO, Luis""