Fig. 1From: Identification of a novel DNMT1 mutation in a Chinese patient with hereditary sensory and autonomic neuropathy type IEDiffuse brain and cerebellar atrophy, especially the cerebellum. Sulcus inbilateral frontal, parietal, occipital lobe increases in width and depth (a-d: T1 weighted imaging, e-h: T2 weighted imaging, i-l: Fluid attenuated inversion recovery)Back to article page