Fig. 3From: A novel ELOVL4 variant, L168S, causes early childhood-onset Spinocerebellar ataxia-34 and retinal dysfunction: a case reportConfirmation of the NM_022726.3: c.503 T > C de novo variant with Sanger sequencing. (I) index case, (II) father, (III) mother with forward primers (upper electropherogram) and reverse primers (lower electropherogram). The variant is between black lines on the 503 positionBack to article page