A Functional Null Mutation of SCN1B in a Patient with Dravet Syndrome-Reference-Cited by-同舟云学术

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

Published:2009-08-26 Issue:34 Volume:29 Page:10764-10778
ISSN:0270-6474
Container-title:Journal of Neuroscience
language:en
Short-container-title:Journal of Neuroscience

Author:

Patino G. A.,Claes L. R. F.,Lopez-Santiago L. F.,Slat E. A.,Dondeti R. S. R.,Chen C.,O'Malley H. A.,Gray C. B. B.,Miyazaki H.,Nukina N.,Oyama F.,De Jonghe P.,Isom L. L.

Publisher

Society for Neuroscience

Subject

General Neuroscience

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