Skip to main content
Fig. 2 | BMC Neurology

Fig. 2

From: Adult-onset autosomal dominant spastic paraplegia linked to a GTPase-effector domain mutation of dynamin 2

Fig. 2

Pedigree of the Siberian family with Hereditary spastic paraplegia. Filled symbols indicate individuals affected with HSP; open symbols represent unaffected family members. The p.R719W mutation was identified in the affected family members II:6, III:2, III:3, III:7, IV:1, but the test for the mutation was negative in unaffected individuals III:1, IV:2, IV:3, IV:4

Back to article page