The role of SLC2A1 mutations in myoclonic astatic epilepsy and absence epilepsy, and the estimated frequency of GLUT1 deficiency syndrome.
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| Description | scientific article published on 5 November 2015 |
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author: Federico Zara Renzo Guerrini Rikke S Møller Pasquale Striano Michael Simpson Niels Tommerup |
| Publication date | November 5, 2015 |
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