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Q37089623-4951E726-3B4C-4041-892A-3C73A9E004A5
Q37089623-4951E726-3B4C-4041-892A-3C73A9E004A5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37089623-4951E726-3B4C-4041-892A-3C73A9E004A5
hnRNP H enhances skipping of a nonfunctional exon P3A in CHRNA1 and a mutation disrupting its binding causes congenital myasthenic syndrome
P1433
Q37089623-4951E726-3B4C-4041-892A-3C73A9E004A5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37089623-4951E726-3B4C-4041-892A-3C73A9E004A5
rank
NormalRank
type
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Statement
wasDerivedFrom
37f77e0ed667969911e7dc86f13c5fc2393f533e
P1433
Human Molecular Genetics