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Q36827111-2D828665-465D-4612-81C9-CA780490AA2F
Q36827111-2D828665-465D-4612-81C9-CA780490AA2F
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http://www.wikidata.org/entity/statement/Q36827111-2D828665-465D-4612-81C9-CA780490AA2F
High-throughput analyses of hnRNP H1 dissects its multi-functional aspect.
P2860
Q36827111-2D828665-465D-4612-81C9-CA780490AA2F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36827111-2D828665-465D-4612-81C9-CA780490AA2F
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wasDerivedFrom
55096ed916940e2075983a720e3ea20273efe065
P2860
hnRNP H enhances skipping of a nonfunctional exon P3A in CHRNA1 and a mutation disrupting its binding causes congenital myasthenic syndrome