(Q38958438)
Statements
1 reference
Neurologic Phenotypes Associated with Mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR1, and IFIH1: Aicardi-Goutières Syndrome and Beyond (English)
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John H Livingston
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19 September 2016
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47
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6
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355-360
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Identifiers
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1 reference