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10.15844/pedneurbriefs-30-9-1

http://scihub22266oqcxt.onion/10.15844/pedneurbriefs-30-9-1
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C5027035!5027035 !27651130
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suck abstract from ncbi


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pmid27651130
      Pediatr+Neurol+Briefs 2016 ; 30 (9 ): 36
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  • Genetic Testing Requires NGS and Sanger Methodologies #MMPMID27651130
  • Jennings LJ ; Kirschmann D
  • Pediatr Neurol Briefs 2016[Sep]; 30 (9 ): 36 PMID27651130 show ga
  • 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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