Figure 1From: Autosomal recessive cerebellar ataxia caused by mutations in the PEX2 geneBrain T-1 weighted magnetic resonance imaging showing marked cerebellar atrophy in P1 at the age of 9 years (panel A) and 14 years (panel B), and in P2 at the age of 18 years (panel C). Panel D shows a normal brain MRI in a 16 years-old control.Back to article page