Reiss, J., Gross-Hardt, S., Christensen, E., Schmidt, P., Mendel, R. R., & Schwarz, G. (2001). A Mutation in the Gene for the Neurotransmitter Receptor–Clustering Protein Gephyrin Causes a Novel Form of Molybdenum Cofactor Deficiency. The American Society of Human Genetics.

Reiss, Jochen, Sigrid Gross-Hardt, Ernst Christensen, Peter Schmidt, Ralf R. Mendel, und Günter Schwarz. A Mutation in the Gene for the Neurotransmitter Receptor–Clustering Protein Gephyrin Causes a Novel Form of Molybdenum Cofactor Deficiency. The American Society of Human Genetics, 2001.

Reiss, Jochen, et al. A Mutation in the Gene for the Neurotransmitter Receptor–Clustering Protein Gephyrin Causes a Novel Form of Molybdenum Cofactor Deficiency. The American Society of Human Genetics, 2001.