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Unusual pure motor axonal neuropathy in a Burmese family with galactosialidosis

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Journal of Inherited Metabolic Disease

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REFERENCES

  • D'Azzo A, Hoogeveen A, Reuser AJ, Robinson D, Galjaard H (1982) Molecular defect in combined beta-galactosidase and neuraminidase deficiency in man. Proc Natl Acad Sci USA 79: 4535.

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  • Sips HJ, de Wit-Verbeek E, de Wit J, Westerveld A, Galjaard H (1985) The chromosomal localisation of human beta-galactosidase revisited: a locus for beta-galactosidase on human chromosome 3 and for its protective protein on human chromosome 22. Hum Genet 69: 340.

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Authors
  1. E. K. Tan
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  2. M. C. Wong
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  3. I. Ng
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  4. S. H. Teo
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  5. Y. L. Lo
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  6. M. M. Cho
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Tan, E.K., Wong, M.C., Ng, I. et al. Unusual pure motor axonal neuropathy in a Burmese family with galactosialidosis. J Inherit Metab Dis 21, 869–870 (1998). https://doi.org/10.1023/A:1005431021025

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  • DOI: https://doi.org/10.1023/A:1005431021025

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