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Q43871750-464C9C01-379C-4A6A-8DAD-E9E9DFC45345
Q43871750-464C9C01-379C-4A6A-8DAD-E9E9DFC45345
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http://www.wikidata.org/entity/statement/Q43871750-464C9C01-379C-4A6A-8DAD-E9E9DFC45345
RSK2 mutation co-segregates with X-linked intellectual disability and attenuated Coffin-Lowry phenotype in a three-generation family.
P2860
Q43871750-464C9C01-379C-4A6A-8DAD-E9E9DFC45345
BestRank
Statement
http://www.wikidata.org/entity/statement/Q43871750-464C9C01-379C-4A6A-8DAD-E9E9DFC45345
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type
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wasDerivedFrom
a9e0db91f66cdebf4d52597b07a5f883a2832f33
P2860
Rapid immunoblot and kinase assay tests for a syndromal form of X linked mental retardation: Coffin-Lowry syndrome