Article info
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Novel mutations in COX15 in a long surviving Leigh syndrome patient with cytochrome c oxidase deficiency
- Correspondence to: Massimo Zeviani Department of Molecular Neurogenetics, Istituto Nazionale Neurologico “C. Besta”, via Libero Temolo, 4 20126 Milano, Italy; zevianiistituto-besta.it
Citation
Novel mutations in COX15 in a long surviving Leigh syndrome patient with cytochrome c oxidase deficiency
Publication history
- Accepted December 17, 2004
- Revised December 10, 2004
- First published April 29, 2005.
Online issue publication
April 27, 2016
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Copyright 2005 Journal of Medical Genetics