Müller, Franz-Josef Dept. of Genome Regulation (Head: Alexander Meissner), Max Planck Institute for Molecular Genetics, Max Planck Society;
Vögtle.pdf (Verlagsversion), 3MB
Vögtle, F.-N., Brändl, B., Larson, A., Pendziwiat, M., Friederich, M. W., White, S. M., et al. (2018). Mutations in PMPCB Encoding the Catalytic Subunit of the Mitochondrial Presequence Protease Cause Neurodegeneration in Early Childhood. American Journal of Human Genetics, 102(4), 557-573. doi:10.1016/j.ajhg.2018.02.014.