[HTML][HTML] SCN1A Mutation—Beyond Dravet Syndrome: A Systematic Review and Narrative Synthesis
J Ding, X Li, H Tian, L Wang, B Guo, Y Wang… - Frontiers in …, 2021 - frontiersin.org
Background: SCN1A is one of the most common epilepsy genes. About 80% of SCN1A
gene mutations cause Dravet syndrome (DS), which is a severe and catastrophic epileptic …
gene mutations cause Dravet syndrome (DS), which is a severe and catastrophic epileptic …
[HTML][HTML] SCN1A Mutation—Beyond Dravet Syndrome: A Systematic Review and Narrative Synthesis
J Ding, X Li, H Tian, L Wang, B Guo, Y Wang… - Frontiers in …, 2021 - ncbi.nlm.nih.gov
Background: SCN1A is one of the most common epilepsy genes. About 80% of SCN1A
gene mutations cause Dravet syndrome (DS), which is a severe and catastrophic epileptic …
gene mutations cause Dravet syndrome (DS), which is a severe and catastrophic epileptic …
SCN1A Mutation-Beyond Dravet Syndrome: A Systematic Review and Narrative Synthesis.
J Ding, X Li, H Tian, L Wang, B Guo, Y Wang… - Frontiers in …, 2021 - europepmc.org
Background: SCN1A is one of the most common epilepsy genes. About 80% of SCN1A
gene mutations cause Dravet syndrome (DS), which is a severe and catastrophic epileptic …
gene mutations cause Dravet syndrome (DS), which is a severe and catastrophic epileptic …
SCN1A Mutation-Beyond Dravet Syndrome: A Systematic Review and Narrative Synthesis
J Ding, X Li, H Tian, L Wang, B Guo… - Frontiers in …, 2021 - pubmed.ncbi.nlm.nih.gov
Background: SCN1A is one of the most common epilepsy genes. About 80% of SCN1A
gene mutations cause Dravet syndrome (DS), which is a severe and catastrophic epileptic …
gene mutations cause Dravet syndrome (DS), which is a severe and catastrophic epileptic …
[HTML][HTML] SCN1A Mutation—Beyond Dravet Syndrome: A Systematic Review and Narrative Synthesis
J Ding, X Li, H Tian, W Li, F Wang, T Sun - Frontiers in Neurology, 2021 - frontiersin.org
Background: SCN1A is one of the most common epilepsy genes. About 80% of SCN1A
gene mutations cause Dravet syndrome (DS), which is a severe and catastrophic epileptic …
gene mutations cause Dravet syndrome (DS), which is a severe and catastrophic epileptic …
SCN1A Mutation-Beyond Dravet Syndrome: A Systematic Review and Narrative Synthesis.
J Ding, X Li, H Tian, L Wang, B Guo, Y Wang… - Frontiers in …, 2021 - europepmc.org
Background: SCN1A is one of the most common epilepsy genes. About 80% of SCN1A
gene mutations cause Dravet syndrome (DS), which is a severe and catastrophic epileptic …
gene mutations cause Dravet syndrome (DS), which is a severe and catastrophic epileptic …