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New loci
Original article
Old gene, new phenotype: mutations in heparan sulfate synthesis enzyme, EXT2 leads to seizure and developmental disorder, no exostoses
- Correspondence to Professor Robert A Hegele, Blackburn Cardiovascular Genetics Laboratory, 4288A-1151 Richmond St North, Robarts Research Institute, Western University, London, Ontario, Canada N6A 5B7; hegele{at}robarts.ca
Citation
Old gene, new phenotype: mutations in heparan sulfate synthesis enzyme, EXT2 leads to seizure and developmental disorder, no exostoses
Publication history
- Received May 22, 2015
- Accepted July 6, 2015
- First published August 5, 2015.
Online issue publication
April 27, 2016
Article Versions
- Previous version (27 April 2016).
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