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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

Steven Mumm

Division of Bone and Mineral Diseases

Washington University School of Medicine at Barnes-Jewish Hospital

St. Louis

Missouri 63110



Name/email consistency: high



  • Division of Bone and Mineral Diseases, Washington University School of Medicine at Barnes-Jewish Hospital, St. Louis, Missouri 63110, USA. 2000 - 2002


  1. Denaturing gradient gel electrophoresis analysis of the tissue nonspecific alkaline phosphatase isoenzyme gene in hypophosphatasia. Mumm, S., Jones, J., Finnegan, P., Henthorn, P.S., Podgornik, M.N., Whyte, M.P. Mol. Genet. Metab. (2002) [Pubmed]
  2. The sedlin gene for spondyloepiphyseal dysplasia tarda escapes X-inactivation and contains a non-canonical splice site. Mumm, S., Zhang, X., Vacca, M., D'Esposito, M., Whyte, M.P. Gene (2001) [Pubmed]
  3. A five-base pair deletion in the sedlin gene causes spondyloepiphyseal dysplasia tarda in a six-generation Arkansas kindred. Mumm, S., Christie, P.T., Finnegan, P., Jones, J., Dixon, P.H., Pannett, A.A., Harding, B., Gottesman, G.S., Thakker, R.V., Whyte, M.P. J. Clin. Endocrinol. Metab. (2000) [Pubmed]
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