Fig. 2From: Lack of mitochondrial complex I assembly factor NDUFAF2 results in a distinctive infantile-onset brainstem neurodegenerative disease with early lethalityChromosome microarray analysis (CMA) of P4 and her parents. Interstitial deletion of 142 kb is seen in a homozygous state in the patient (lower panel) and in a heterozygous state in both parents (upper and middle panels)Back to article page