Jochen Reiss
Institut für Humangenetik
Universitätsmedizin Göttingen
Germany
Name/email consistency: high
- Molybdenum cofactor deficiency: Mutations in GPHN, MOCS1, and MOCS2. Reiss, J., Hahnewald, R. Hum. Mutat. (2011)
- The pathogenesis of molybdenum cofactor deficiency, its delay by maternal clearance, and its expression pattern in microarray analysis. Reiss, J., Bonin, M., Schwegler, H., Sass, J.O., Garattini, E., Wagner, S., Lee, H.J., Engel, W., Riess, O., Schwarz, G. Mol. Genet. Metab. (2005)
- Mutations in the molybdenum cofactor biosynthetic genes MOCS1, MOCS2, and GEPH. Reiss, J., Johnson, J.L. Hum. Mutat. (2003)
- Human molybdopterin synthase gene: genomic structure and mutations in molybdenum cofactor deficiency type B. Reiss, J., Dorche, C., Stallmeyer, B., Mendel, R.R., Cohen, N., Zabot, M.T. Am. J. Hum. Genet. (1999)
- Molybdenum cofactor deficiency: first prenatal genetic analysis. Reiss, J., Christensen, E., Dorche, C. Prenat. Diagn. (1999)
- Mutations in a polycistronic nuclear gene associated with molybdenum cofactor deficiency. Reiss, J., Cohen, N., Dorche, C., Mandel, H., Mendel, R.R., Stallmeyer, B., Zabot, M.T., Dierks, T. Nat. Genet. (1998)
- Genomic structure and mutational spectrum of the bicistronic MOCS1 gene defective in molybdenum cofactor deficiency type A. Reiss, J., Christensen, E., Kurlemann, G., Zabot, M.T., Dorche, C. Hum. Genet. (1998)
