TY - JOUR AU - Janer, A; Antonicka, H; Lalonde, E TI - An RMND1 Mutation causes encephalopathy associated with multiple oxidative phosphorylation complex deficiencies and a mitochondrial translation defect JO - Am J Hum Genet IS - 04 VL - 91 PY - 2012 DO - 10.1016/j.ajhg.2012.08.020 L3 - PubMed-ID: 23022098 SP - 737 EP - 743 ER -