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. Author manuscript; available in PMC: 2010 Feb 1.
Published in final edited form as: Arch Neurol. 2009 Feb;66(2):238–243. doi: 10.1001/archneurol.2008.585

Figure 2.

Figure 2

One of 13 kindreds studied with hereditary brachial plexus neuropathy (H-BPN) identified with SEPT-9 mutation. Top, 5-generation kindred affected by recurrent attacks of brachial plexus neuropathy with apparent dominant inheritance. (bottom, left) Sequencing analysis identifying 262C→T transition leading to Arg88Trp. (bottom, right) Complimentary strand confirmatory pyrosequencing assay showing A and G heterozygous occurrence at base position 262, with kindred evaluation on top and possible combination below.