SCN1A genetic test for Dravet Syndrome (Severe Myoclonic Epilepsy of Infancy and its clinical subtypes) for the use in the diagnosis, prognosis, treatment and management of Dravet Syndrome
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| Description | scientific article published on April 25, 2013 |
| Author/s |
author: Sameer M Zuberi |
| Publication date | April 25, 2013 |
| Language | English |
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| Access work |
https://doi.org/10.1371/currents.eogt.c553b83d745dd79bfb61eaf35e522b0b |
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| Missing/wrong data? | Edit Wikidata item |