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SCN2A mutation in an infant with Ohtahara syndrome and neuroimaging findings: expanding the phenotype of neuronal migration disorders

Victoria Vlachou; Line Larsen; Efterpi Pavlidou; Naila Ismayilova; N. D. Mazarakis; Mantha Pantazi; Kshitij Mankad; Maria Kinali
Journal of Genetics · Vol. 98, Issue 2 · 2019
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Bibliographic Information

JournalJournal of Genetics
PublisherSpringer
Publication Date2019-06-01
Publication Year2019
Volume98
Issue2
Document TypeJournal Article
eISSN0973-7731
DOI10.1007/s12041-019-1104-3

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NARA Access Coverage1910-01-01~Current
Journal Homepagehttps://www.springer.com/journal/12041
Publisher PageOpen Publisher Page
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