Mutations in C12orf65 in Patients with Encephalomyopathy and a Mitochondrial Translation Defect

H. Antonicka, E. Ostergaard, F. Sasarman, W. Weraarpachai, F. Wibrand, A.M.B. Pedersen, R.J. Rodenburg, M.S. van der Knaap, J.A.M. Smeitink, ZM Chrzanowska-Lightowlers, E.A. Shoubridge

Research output: Contribution to journalArticleAcademicpeer-review

Original languageUndefined/Unknown
Pages (from-to)115-122
JournalAmerican journal of human genetics
Volume87
Issue number1
DOIs
Publication statusPublished - 2010

Cite this

Antonicka, H., Ostergaard, E., Sasarman, F., Weraarpachai, W., Wibrand, F., Pedersen, A. M. B., ... Shoubridge, E. A. (2010). Mutations in C12orf65 in Patients with Encephalomyopathy and a Mitochondrial Translation Defect. American journal of human genetics, 87(1), 115-122. https://doi.org/10.1016/j.ajhg.2010.06.004