Items where Author is "Rutsch, Frank"
Number of items: 4. 2011Rutsch, Frank and Gailus, Susann and Suormala, Terttu and Fowler, Brian. (2011) LMBRD1: the gene for the cblF defect of vitamin B₁₂ metabolism. Journal of inherited metabolic disease, Vol. 34, no. 1. pp. 121-126. 2010Gailus, Susann and Suormala, Terttu and Malerczyk-Aktas, Ayse Gül and Toliat, Mohammad R. and Wittkampf, Tanja and Stucki, Martin and Nürnberg, Peter and Fowler, Brian and Hennermann, Julia B. and Rutsch, Frank. (2010) A novel mutation in LMBRD1 causes the cblF defect of vitamin B(12) metabolism in a Turkish patient. Journal of Inherited Metabolic Disease, Vol. 33, no. 1. pp. 17-24. Gailus, Susann and Höhne, Wolfgang and Gasnier, Bruno and Nürnberg, Peter and Fowler, Brian and Rutsch, Frank. (2010) Insights into lysosomal cobalamin trafficking : lessons learned from cblF disease. Journal of molecular medicine, Vol. 88, no. 5. pp. 459-466. 2009Rutsch, Frank and Gailus, Susann and Miousse, Isabelle R. and Suormala, Terttu and Sagné, Corinne and Toliat, Mohammad Reza and Nürnberg, Gudrun and Wittkampf, Tanja and Buers, Insa and Sharifi, Azita and Stucki, Martin and Becker, Christian and Baumgartner, Matthias and Robenek, Horst and Marquardt, Thorsten and Höhne, Wolfgang and Gasnier, Bruno and Rosenblatt, David S. and Fowler, Brian and Nürnberg, Peter. (2009) Identification of a putative lysosomal cobalamin exporter altered in the cblF defect of vitamin B12 metabolism. Nature genetics, Vol. 41, H. 2. pp. 234-239. |
