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Brown, Robert
One or more keywords matched the following items that are connected to
Brown, Robert
Item Type
Name
Academic Article
Association of UBQLN1 mutation with Brown-Vialetto-Van Laere syndrome but not typical ALS.
Concept
Bulbar Palsy, Progressive
Academic Article
Further analysis of KIFAP3 gene in ALS patients from Switzerland and Sweden.
Search Criteria
Bulbar Palsy Progressive