Journal: Experimental and Therapeutic Medicine
Article Title: Novel PRRT2 gene variants identified in paroxysmal kinesigenic dyskinesia and benign familial infantile epilepsy in Chinese families
doi: 10.3892/etm.2021.9935
Figure Lengend Snippet: (A) Sequencing chromatograms indicating the PRRT2 variants detected in family A. (a) The mutated sequence and (b) the wild-type sequence. (B) Sequencing chromatograms displaying the PRRT2 variants detected in family B. (a) The mutated sequence and (b) the wild-type sequence. (C) Sequencing chromatograms indicating the PRRT2 variants detected in family C. (a) The mutated sequence and (b) the wild-type sequence. The red arrows indicate the variant site. Position numbers are displayed above the sequences. PRRT2, proline-rich transmembrane protein 2.
Article Snippet: Genomic DNA reference sequences of candidate gene PRRT2 (NM_001256442.2) were obtained from the University of California Santa Cruz (UCSC) Genome Browser database ( http://genome.ucsc.edu/ ).
Techniques: Sequencing, Variant Assay