Relevant conflicts of interest/financial disclosures: Nothing to report.
Article first published online: 2 JAN 2013
Copyright © 2012 Movement Disorder Society
Volume 27, Issue 14, page 1738, December 2012
How to Cite
Alexoudi, A. and Schneider, S. A. (2012), Mutations in the phospholipid remodeling gene SERAC1 cause MEGDEL syndrome. Mov. Disord., 27: 1738. doi: 10.1002/mds.25228
Wortmann SB, Vaz FM, Gardeitchik T, et al. Mutations in the phospholipid remodeling gene SERAC1 impair mitochondrial function and intracellular cholesterol trafficking and cause dystonia and deafness. Nat Genet. 2012;44:797–802.
- Issue published online: 2 JAN 2013
- Article first published online: 2 JAN 2013
- Manuscript Accepted: 6 SEP 2012
- Manuscript Received: 4 SEP 2012
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