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The c.859G>C variant in the SMN2 gene is associated with types II and III SMA and originates from a common ancestor
- Correspondence to Eduardo F Tizzano, Genetics, Hospital de la Santa Creu i Sant Pau, Sant Antoni Ma. Claret 167, 08025 Barcelona, Spain; etizzano{at}santpau.cat
Citation
The c.859G>C variant in the SMN2 gene is associated with types II and III SMA and originates from a common ancestor
Publication history
- Received March 10, 2010
- Accepted March 16, 2010
- First published June 24, 2010.
Online issue publication
April 27, 2016
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© 2010, 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.