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Q37071684-49DDF2C2-7780-46B4-B148-43AD4D88E5F3
Q37071684-49DDF2C2-7780-46B4-B148-43AD4D88E5F3
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http://www.wikidata.org/entity/statement/Q37071684-49DDF2C2-7780-46B4-B148-43AD4D88E5F3
Delineation of the mechanisms of aberrant splicing caused by two unusual intronic mutations in the RSK2 gene involved in Coffin-Lowry syndrome.
P2860
Q37071684-49DDF2C2-7780-46B4-B148-43AD4D88E5F3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37071684-49DDF2C2-7780-46B4-B148-43AD4D88E5F3
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5f683bbb54f78488e6a70a4205ac033fa6776d3e
P2860
Coffin-Lowry syndrome: clinical aspects at different ages and symptoms in female carriers.