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Molecular defect of caprineN-acetylglucosamine-6-sulphatase deficiency. A single base substitution creates a stop codon in the 5′-region of the coding sequence

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Journal of Inherited Metabolic Disease

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References

  • Robertson DA, Freeman C, Morris CP et al (1992) A cDNA clone for human glucosamine 6-sulfatase reveals differences between arylsulfatases and non-arylsulfatases.Biochem J 288: 539–544.

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  • Thompson JN, Jones MZ, Dawson G, Huffman PS (1992)N-Acetylglucosamine 6-sulphatase deficiency in a nubian goat: a model of Sanfilippo syndrome type D (mucopolysaccharidosis IIID).J Inher Metab Dis 15: 760–768.

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Authors and Affiliations

  1. Department of Pathology, Michigan State University, 48824, East Lansing, MI, USA

    K. T. Cavanagh, J. R. Leipprandt, M. Z. Jones & K. Friderici

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  1. K. T. Cavanagh
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  2. J. R. Leipprandt
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  3. M. Z. Jones
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  4. K. Friderici
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Cavanagh, K.T., Leipprandt, J.R., Jones, M.Z. et al. Molecular defect of caprineN-acetylglucosamine-6-sulphatase deficiency. A single base substitution creates a stop codon in the 5′-region of the coding sequence. J Inherit Metab Dis 18, 96 (1995). https://doi.org/10.1007/BF00711390

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  • DOI: https://doi.org/10.1007/BF00711390

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