Article info

Download PDFPDF
SPTLC1 and RAB7 mutation analysis in dominantly inherited and idiopathic sensory neuropathies
  1. Correspondence to:
 Dr Christopher J Klein
 Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA; klein.christophermayo.edu
View Full Text

Citation

Klein CJ, Wu Y, Kruckeberg KE, et al
SPTLC1 and RAB7 mutation analysis in dominantly inherited and idiopathic sensory neuropathies

Publication history

  • Received July 16, 2004
  • Accepted October 13, 2004
  • Revised September 13, 2004
  • First published June 16, 2005.
Online issue publication 
April 13, 2016

Request permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.