Whole genome sequencing identifies SCN2A...

Epilepsia 2013 / 05 Vol. 54; Iss. 5

Whole genome sequencing identifies SCN2A mutation in monozygotic twins with Ohtahara syndrome and unique neuropathologic findings

Touma, Marlin, Joshi, Mugdha, Connolly, Meghan C., Ellen Grant, P., Hansen, Anne R., Khwaja, Omar, Berry, Gerard T., Kinney, Hannah C., Poduri, Annapurna, Agrawal, Pankaj B.
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Volume:
54
Language:
english
Journal:
Epilepsia
DOI:
10.1111/epi.12137
Date:
May, 2013
File:
PDF, 449 KB
english, 2013
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