These authors contributed equally to this work.
Primary carnitine deficiency: novel mutations and insights into the cardiac phenotype
Version of Record online: 12 MAR 2013
© 2013 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd
Volume 85, Issue 2, pages 127–137, February 2014
How to Cite
Shibbani, K., Fahed, A.C., Al-Shaar, L., Arabi, M., Nemer, G., Bitar, F. and Majdalani, M. (2014), Primary carnitine deficiency: novel mutations and insights into the cardiac phenotype. Clinical Genetics, 85: 127–137. doi: 10.1111/cge.12112
No conflict of interest to declare for all participating authors.
- Issue online: 13 JAN 2014
- Version of Record online: 12 MAR 2013
- Accepted manuscript online: 4 FEB 2013 02:06PM EST
- Manuscript Revised: 22 JAN 2013
- Manuscript Received: 20 DEC 2012
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