Genetic Testing Requires NGS and Sanger Methodologies
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.
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| Päätekijät: | , |
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| Aineistotyyppi: | Kirja |
| Julkaistu: |
Pediatric Neurology Briefs Publishers,
2016-09-01T00:00:00Z.
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Internet
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| Nide 1 | Saatavissa |