Sequencing of <scp>C</scp>harcot–<scp>M</scp>arie–<scp>T</scp>ooth disease genes in a toxic polyneuropathy

Abstract

The results reveal an association of CMT gene allelic variability with susceptibility to CIPN. The findings raise the possibility that other acquired polyneuropathies may also be codetermined by genetic etiological factors, of which some may be related to genes already known to cause the phenotypically related Mendelian disorders of CMT.