Figure 1.

Pedigree of the AMRF family with mutation status. Black symbol: AMRF. Grey symbol: generalized epilepsy and reduction of nerve conduction velocity in the feet. +/+: homozygous mutation, +/-: heterozygous mutation. Symbol #: no information available about genotype status.

Hopfner et al. BMC Neurology 2011 11:134   doi:10.1186/1471-2377-11-134
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