Eveline Jongen

Exome sequencing reveals a novel Moroccan founder mutation in<i>SLC19A3</i>as a new cause of early-childhood fatal Leigh syndrome

Mike Gerards, Rick Kamps, Jo van Oevelen et al. · Brain · 2013 · 93 citations · Full text

The unfolding clinical spectrum of <i>POLG</i> mutations

Marinus J. Blok, B.J.C. van den Bosch, Eveline Jongen et al. · Journal of Medical Genetics · 2009 · 85 citations · Full text

Defective NDUFA9 as a novel cause of neonatally fatal complex I disease

B.J.C. van den Bosch, Mike Gerards, Wim J. Sluiter et al. · Journal of Medical Genetics · 2011 · 52 citations · Full text