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King, Oliver
One or more keywords matched the following items that are connected to
King, Oliver
Item Type
Name
Academic Article
Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS.
Concept
Muscular Dystrophies, Limb-Girdle
Academic Article
Precise therapeutic gene correction by a simple nuclease-induced double-stranded break.
Search Criteria
Limb Girdle Muscular Dystrophies