Publications by authors named "David P Gow"

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A novel DNMT1 mutation associated with early onset hereditary sensory and autonomic neuropathy, cataplexy, cerebellar atrophy, scleroderma, endocrinopathy, and common variable immune deficiency.
Robin Fox, John Ealing, Helen Murphy, David P Gow, David Gosal

J Peripher Nerv Systยท September 2016

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