A new molecular mechanism for severe myoclonic epilepsy of infancy: exonic deletions in SCN1A.
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| Title: | A new molecular mechanism for severe myoclonic epilepsy of infancy: exonic deletions in SCN1A. |
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| Authors: | Mulley JC; Department of Genetic Medicine, Women's and Children's Hospital, North Adelaide, South Australia, 5006 Australia. john.mulley@cywhs.sa.gov.au, Nelson P, Guerrero S, Dibbens L, Iona X, McMahon JM, Harkin L, Schouten J, Yu S, Berkovic SF, Scheffer IE |
| Source: | Neurology [Neurology] 2006 Sep 26; Vol. 67 (6), pp. 1094-5. |
| Publication Type: | Comparative Study; Journal Article; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 0401060 Publication Model: Print Cited Medium: Internet ISSN: 1526-632X (Electronic) Linking ISSN: 00283878 NLM ISO Abbreviation: Neurology Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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