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Short report
Combined malonic and methylmalonic aciduria: exome sequencing reveals mutations in the ACSF3 gene in patients with a non-classic phenotype
- Correspondence to Dr Nancy Braverman, McGill University–Montreal Children's Hospital Research Institute, 4060 Ste-Catherine West, PT-406.2, Montreal, QC H3Z 2Z3, Canada; nancy.braverman{at}mcgill.ca
Citation
Combined malonic and methylmalonic aciduria: exome sequencing reveals mutations in the ACSF3 gene in patients with a non-classic phenotype
Publication history
- Received June 5, 2011
- Revised July 11, 2011
- Accepted July 12, 2011
- First published July 23, 2011.
Online issue publication
April 27, 2016
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