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. Author manuscript; available in PMC: 2015 Aug 1.
Published in final edited form as: Parkinsonism Relat Disord. 2014 May 13;20(8):884–888. doi: 10.1016/j.parkreldis.2014.05.004

Figure 1. Pedigree structures of three kindreds with Perry syndrome.

Figure 1

Panel 1a) includes the pedigree with the DCTN1 p.Y78C (c.233A>G) mutation, and 1b and 1c) pedigrees with the DCTN1 p.G71R (c.211G>A) mutation. Standard symbols were used. Round symbols indicate females, squares males, diagonal lines indicate the individual is deceased. Diamonds were used to disguise gender. The solid arrowhead indicates the proband. Black full-filled symbols indicate individuals who suffered from Perry syndrome. Asterisks indicate that genetic testing for DCTN1 gene mutation was performed.