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doi: 10.1002/rcm.4167
The syndrome is most often caused by mutations in the RECQL4 helicase, a member of the RecQ helicase family, which is involved in DNA repair and replication (Croteau et al
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The pathogenesis of parkinsons disease: a complex interplay between astrocytes, microglia, and T lymphocytes
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The mice were injected intravenously with PBS, Ru(II)-OH, NP2, NP4 (2 mg/kg Ru) on days 1, 4, 7, 10, respectively
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