Fig. 4
From: A case of rapid-onset dystonia-parkinsonism accompanied by pyramidal tract impairment
Next-generation sequencing of the patient and her father. Next-generation sequencing of the patient revealed a heterozygous nucleotide substitution (c.829G > A) in ATP1A3 gene in exon 8 of chromosome 19 (chr19:42489234) (a). Next-generation sequencing of the patient’s father revealed no nucleotide substitution in ATP1A3 gene (b)