Identification of a rare SEPT9 variant in a family with autosomal dominant Charcot-Marie-Tooth disease.

Authors

Grosse GM1, Bauer C2, Kopp B3, Schrader C3, Osmanovic A3.
  1. Department of Neurology, Hannover Medical School, Carl-Neuberg-Str. 1, 30625, Hannover, Germany. grosse.gerrit@mh-hannover.de.
  2. Center for Genomics and Transcriptomics (CeGaT GmbH), Tübingen, Germany.
  3. Department of Neurology, Hannover Medical School, Carl-Neuberg-Str. 1, 30625, Hannover, Germany.