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Metachromatic leukodystrophy

Author: Volkmar Gieselmann
Publisher: London : Henry Stewart Talks, 2007.
Series: Henry Stewart talks., Biomedical & life sciences collection., Protein epidemiology : understanding human diseases at the level of protein structure and function.
Edition/Format:   eVideo : Clipart/images/graphics : EnglishView all editions and formats
Summary:
Audio-visual presentation : Metabolic defect in metachromatic leukodystrophy ; Genetics ; Genotype/phenotype correlations ; Biochemical consequences of selected mutations ; Diganostic problems due to arylsulfatase A pseudodeficiency ; Gene therapy and enzyme replacement trials in an animal model.
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Details

Material Type: Clipart/images/graphics, Internet resource, Videorecording
Document Type: Internet Resource, Computer File, Visual material
All Authors / Contributors: Volkmar Gieselmann
OCLC Number: 310380992
Notes: Title from title frames.
Animated audio-visual presentation with synchronized narration.
Description: 1 streaming video file (49 min.) : digital, mono, SWF file, sound, color.
Details: Mode of access: World Wide Web.; System requirements: Operating System: PC Windows 2000+, Mac OSX+ 3.2. Browser Compatibility: IE6+, Firefox 2+, Opera 9+, Safari 2+ 3.3. Browser settings: enable JavaScript, enable popups from the Henry Stewart Talks site. 3.4. Required Browser Plugins & Viewers: Adobe (Macromedia) Flash Player 7+, Adobe Acrobat Reader 6.0+.
Contents: Metabolic defect in metachromatic leukodystrophy --
Genetics --
Genotype/phenotype correlations --
Biochemical consequences of selected mutations --
Diganostic problems due to arylsulfatase A pseudodeficiency --
Gene therapy and enzyme replacement trials in an animal model.
Series Title: Henry Stewart talks., Biomedical & life sciences collection., Protein epidemiology : understanding human diseases at the level of protein structure and function.
Responsibility: Volkmar Gieselmann.
More information:

Abstract:

Audio-visual presentation : Metabolic defect in metachromatic leukodystrophy ; Genetics ; Genotype/phenotype correlations ; Biochemical consequences of selected mutations ; Diganostic problems due to arylsulfatase A pseudodeficiency ; Gene therapy and enzyme replacement trials in an animal model.

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