Citations for
1COXPD11, RMND1
Infantile Encephaloneuromyopathy and Defective Mitochondrial Translation Are Due to a Homozygous RMND1 Mutation.
Garcia-Diaz B, Barros MH, Sanna-Cherchi S, Emmanuele V, Akman HO, Ferreiro-Barros CC, Horvath R, Tadesse S, El Gharaby N, Dimauro S, De Vivo DC, Shokr A, Hirano M, Quinzii CM.
Am J Hum Genet 91(4):729-36. doi: 10.1016/j.ajhg.2012.08.019. Epub 2012 Sep 27. 2012
2COXPD11, RMND1
An RMND1 Mutation Causes Encephalopathy Associated with Multiple Oxidative Phosphorylation Complex Deficiencies and a Mitochondrial Translation Defect.
Janer A, Antonicka H, Lalonde E, Nishimura T, Sasarman F, Brown GK, Brown RM, Majewski J, Shoubridge EA.
Am J Hum Genet 91(4):737-43. doi: 10.1016/j.ajhg.2012.08.020. Epub 2012 Sep 27. 2012