A new molecular mechanism for severe myoclonic epilepsy of infancy: Exonic deletions in SCN1A (Q58417059)
scientific article published on 01 September 2006
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Current Data About A new molecular mechanism for severe myoclonic epilepsy of infancy: Exonic deletions in SCN1A
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(P1476) "A new molecular mechanism for severe myoclonic epilepsy of infancy: exonic deletions in SCN1A" (language: en)
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(P2093) Mulley JC
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Nelson P
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Guerrero S
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Dibbens L
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Iona X
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Harkin L
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(P813) Thursday, December 19, 2019

Schouten J
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(P813) Thursday, December 19, 2019

Yu S
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other details
description scientific article published on 01 September 2006

External Links
(P356) 10.1212/01.WNL.0000237322.04338.2B
(P698) 17000989