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pro vyhledávání: '"Dawn Kirschmann"'
Autor:
Lawrence J. Jennings, Dawn Kirschmann
Publikováno v:
Pediatric Neurology Briefs, Vol 30, Iss 9 (2016)
Investigators from the EuroEPINOMICS rare epilepsy syndromes Dravet working group performed whole-exome sequencing on 31 trios that had been reported negative for SCN1A mutations by Sanger sequencing.
Externí odkaz:
https://doaj.org/article/6bc86fab550548ca853fd48478b54618