Molecular analysis of SUMF1 mutations: stability and residual activity of mutant formylglycine-generating enzyme determine disease severity in multiple sulfatase deficiency

Schlotawa L, Steinfeld R, von Figura K, Dierks T, Gärtner J (2008)
Human Mutation 29(1).

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Schlotawa L, Steinfeld R, von Figura K, Dierks T, Gärtner J. Molecular analysis of SUMF1 mutations: stability and residual activity of mutant formylglycine-generating enzyme determine disease severity in multiple sulfatase deficiency. Human Mutation. 2008;29(1).
Schlotawa, L., Steinfeld, R., von Figura, K., Dierks, T., & Gärtner, J. (2008). Molecular analysis of SUMF1 mutations: stability and residual activity of mutant formylglycine-generating enzyme determine disease severity in multiple sulfatase deficiency. Human Mutation, 29(1).
Schlotawa, L., Steinfeld, R., von Figura, K., Dierks, T., and Gärtner, J. (2008). Molecular analysis of SUMF1 mutations: stability and residual activity of mutant formylglycine-generating enzyme determine disease severity in multiple sulfatase deficiency. Human Mutation 29.
Schlotawa, L., et al., 2008. Molecular analysis of SUMF1 mutations: stability and residual activity of mutant formylglycine-generating enzyme determine disease severity in multiple sulfatase deficiency. Human Mutation, 29(1).
L. Schlotawa, et al., “Molecular analysis of SUMF1 mutations: stability and residual activity of mutant formylglycine-generating enzyme determine disease severity in multiple sulfatase deficiency”, Human Mutation, vol. 29, 2008.
Schlotawa, L., Steinfeld, R., von Figura, K., Dierks, T., Gärtner, J.: Molecular analysis of SUMF1 mutations: stability and residual activity of mutant formylglycine-generating enzyme determine disease severity in multiple sulfatase deficiency. Human Mutation. 29, (2008).
Schlotawa, Lars, Steinfeld, Robert, von Figura, Kurt, Dierks, Thomas, and Gärtner, Jutta. “Molecular analysis of SUMF1 mutations: stability and residual activity of mutant formylglycine-generating enzyme determine disease severity in multiple sulfatase deficiency”. Human Mutation 29.1 (2008).
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