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Original article
A founder mutation in Vps37A causes autosomal recessive complex hereditary spastic paraparesis
- Correspondence to Dr Tzipora C Falik-Zaccai, Institute of Human Genetics, Western Galilee Hospital-Naharia, Israel; falikmd.genetics{at}gmail.com
Citation
A founder mutation in Vps37A causes autosomal recessive complex hereditary spastic paraparesis
Publication history
- Received January 3, 2012
- Revised May 14, 2012
- Accepted May 17, 2012
- First published June 20, 2012.
Online issue publication
December 21, 2023
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© 2012, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.