Mitochondrial phenylalanyl-tRNA synthetase mutations underlie fatal infantile Alpers encephalopathyJenni M. Elo, Anu Suomalainen, Alexandra Götz et al.|Human Molecular Genetics|2012Cited by 167
Whole-exome sequencing identifies a mutation in the mitochondrial ribosome protein MRPL44 to underlie mitochondrial infantile cardiomyopathyChristopher J. Carroll, Anu Suomalainen, Pirjo Isohanni et al.|Journal of Medical Genetics|2013Cited by 103