Fig. 1From: A novel homozygous mutation in TRAPPC9 gene causing autosomal recessive non-syndromic intellectual disabilityBrain MRI (T1) of patient one showing mild cortical and cerebellar atrophy, white matter abnormality and thin corpus callosum (A: T1 (sagittal section), B: T2 (coronal section), C: T1 (cross section), D: T2 (cross section))Back to article page