Cite
MLA Citation
Robin Fox et al.. “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, vol. 21, no. 3, 2016, pp. 150–153. http://access.bl.uk/ark:/81055/vdc_100035783418.0x000019