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TSPYL4 gene

Known as: dJ486I3.2, KIAA0721, TSPYL4 
 
National Institutes of Health

Papers overview

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2019
2019
To help provide evidence for prognosis prediction and personalized targeted therapy for patients with head and neck squamous cell… Expand
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2016
2016
Purpose & Methods: We performed whole-exome sequencing in 6 SCN1A-negative patients with Dravet syndrome in order to identify… Expand
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2012
2012
BACKGROUND Dravet syndrome is a severe form of epilepsy. Majority of patients have a mutation in SCN1A gene, which encodes a… Expand
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2012
2012
Background: Dravet syndrome is a severe form of epilepsy. Majority of patients have a mutation in SCN1A gene, which encodes a… Expand
  • table 2
  • figure 1
  • table 3
  • table 4
  • figure 2
Is this relevant?