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Molecular and Chemical Neuropathology

, Volume 27, Issue 1, pp 67–67 | Cite as

Metachromatic leukodystrophy among Navajo Indians and Eskimos

  • David Wenger
Transcript of the Scientific Symposium The MRI Suggests a Leukodystrophy, but Tests Are Negative—What Should We Do? Probing White-Matter Disorders Abridged Transcript of a Conference Sponsored by the United Leukodystrophy Foundation, held at Kishwaukee Community Hospital, De Kalb, IL, May 7–9, 1994 Session V: Classified Leukodystrophies
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Keywords

Chemical Neuropathology Splice Site Mutation Exact Family Relationship Leukodystrophy Arylsulfatase 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

References

  1. Pastor-Solor N. M., Rafi M. A., Hoffman J. D., Hu D., and Wenger D. A. (1994) Metachromatic leukodystrophy in the Navajo Indian population: A splice site mutation in Intron 4 of the arylsulfatase A gene.Hum. Mutat. 4, 199–207.CrossRefGoogle Scholar
  2. Pastor-Solor N. M., Schertz E. M., Rafi M. A., deGala G., and Wenger D. A. (in press) Metachromatic leukodystrophy among Southern Eskimos: Molecular and genetic studies.J. Inher. Metab. Dis. Google Scholar

Copyright information

© Humana Press Inc. 1996

Authors and Affiliations

  • David Wenger

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