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
Issue number1
Publication statusPublished - 2010

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