Lühl, S., Bode, H., Schlötzer, W., Bartsakoulia, M., Horvath, R., Abicht, A., . . . Grünert, S. C. (2016). Novel homozygous RARS2 mutation in two siblings without pontocerebellar hypoplasia – further expansion of the phenotypic spectrum. BMC.

Lühl, S., H. Bode, W. Schlötzer, M. Bartsakoulia, R. Horvath, A. Abicht, M. Stenzel, J. Kirschner, và S. C. Grünert. Novel Homozygous RARS2 Mutation in Two Siblings Without Pontocerebellar Hypoplasia – Further Expansion of the Phenotypic Spectrum. BMC, 2016.

Lühl, S., et al. Novel Homozygous RARS2 Mutation in Two Siblings Without Pontocerebellar Hypoplasia – Further Expansion of the Phenotypic Spectrum. BMC, 2016.