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Q39625401-3ED2B2B3-C8F5-48FB-8B91-46877F9A4997
Q39625401-3ED2B2B3-C8F5-48FB-8B91-46877F9A4997
BestRank
Statement
http://www.wikidata.org/entity/statement/Q39625401-3ED2B2B3-C8F5-48FB-8B91-46877F9A4997
SMN2 exon 7 splicing is inhibited by binding of hnRNP A1 to a common ESS motif that spans the 3' splice site.
P2860
Q39625401-3ED2B2B3-C8F5-48FB-8B91-46877F9A4997
BestRank
Statement
http://www.wikidata.org/entity/statement/Q39625401-3ED2B2B3-C8F5-48FB-8B91-46877F9A4997
rank
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type
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wasDerivedFrom
fb494d7b94bc44bee5daf1a60c42ab946ff41f83
P2860
hnRNP H enhances skipping of a nonfunctional exon P3A in CHRNA1 and a mutation disrupting its binding causes congenital myasthenic syndrome