DOI:
10.1055/s-00029030
Journal of Pediatric Neurology
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References
Livingston JH, Crow YJ.
Neurologic phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR1, and IFIH1: Aicardi–Goutieres syndrome and beyond.
Neuropediatrics 2016;
47 (06) 355-360
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