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Table 2 Intersection-comparisons of OXR1 deficiency disease and other neurological developmental diseases

From: A loss-of-function mutation in human Oxidation Resistance 1 disrupts the spatial–temporal regulation of histone arginine methylation in neurodevelopment

  1. #The representation factors and relevant probability are calculated by http://nemates.org/MA/progs/overlap_stats.html. All representation factors > 1
  2. $ DEGs,differentially expressed genes of Neu_OXR1ΔEx18 vs. Neu_CTRL
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Genome Biology

ISSN: 1474-760X

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