Fig. 4From: A case report of SPG11 mutations in a Chinese ARHSP-TCC familySanger sequencing of exon 7 (c.1551_1552delTT) containing a TT deletion in SPG11 in an affected individual (a) and unaffected individual (b). Sanger sequencing of a splice site mutation (c.5867-1G > T (IVS30-1G > T)) in intron 30 of SPG11 in an affected individual (c) and control, unaffected (d)Back to article page