Search Results - "Muller, V.J."

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  1. 1

    Identification and molecular characterization of α‐L‐iduronidase mutations present in mucopolysaccharidosis type I patients undergoing enzyme replacement therapy by Yogalingam, G., Guo, X.‐H., Muller, V.J., Brooks, D.A., Clements, P.R., Kakkis, E.D., Hopwood, J.J.

    Published in Human mutation (01-09-2004)
    “…Mucopolysaccharidosis type I (MPS I) is an autosomal recessive lysosomal storage disorder caused by a deficiency of α‐L‐iduronidase (IDUA). Mutations in the…”
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    Journal Article
  2. 2

    Mucopolysaccharidosis IIIA (Sanfilippo syndrome) in a New Zealand Huntaway dog with ataxia by Jolly, R.D., Allan, F.J., Collett, M.G., Rozaklis, T., Muller, V.J., Hopwood, J.J.

    Published in New Zealand veterinary journal (01-10-2000)
    “…Aim: To investigate the nature of a progressive ataxia in a New Zealand Huntaway dog. Methods: The affected dog was examined clinically before being humanely…”
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    Journal Article
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    "Whey" proteins of milk of the red (Macropus rufus) and eastern grey (Macropus giganteus) kangaroo by McKenzie, H A, Muller, V J, Treacy, G B

    “…1. A comparison is made of gel electrophoretic patterns of the "whey" proteins of the milk of red (Macropus rufus) and eastern grey (Macropus giganteus)…”
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