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Q37071684-1BC8CC1E-C9D3-4170-8642-F33867925BEA
Q37071684-1BC8CC1E-C9D3-4170-8642-F33867925BEA
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http://www.wikidata.org/entity/statement/Q37071684-1BC8CC1E-C9D3-4170-8642-F33867925BEA
Delineation of the mechanisms of aberrant splicing caused by two unusual intronic mutations in the RSK2 gene involved in Coffin-Lowry syndrome.
P2860
Q37071684-1BC8CC1E-C9D3-4170-8642-F33867925BEA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37071684-1BC8CC1E-C9D3-4170-8642-F33867925BEA
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5f683bbb54f78488e6a70a4205ac033fa6776d3e
P2860
Correction of disease-associated exon skipping by synthetic exon-specific activators.