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Neonatal seizures associated with a severe neonatal myoclonus like dyskinesia due to a familial KCNQ2 gene mutation
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| Abstract |
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| Language |
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English
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| Source (journal) |
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European journal of paediatric neurology. - London | |
| Publication |
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London : 2012
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| ISSN |
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1090-3798
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| Volume/pages |
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16:4(2012), p. 356-360
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| ISI |
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000306204300005
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