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APA Citation
Fox, R., Ealing, J., Murphy, H., Gow, D. P., & Gosal, D. (2016). a novel DNMT1 mutation associated with early onset hereditary sensory and autonomic neuropathy, cataplexy, cerebellar atrophy, scleroderma, endocrinopathy, and common variable immune deficiency. Journal of the peripheral nervous system, 21(3), 150–153. http://access.bl.uk/ark:/81055/vdc_100035783418.0x000019