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Q30165499-9201187A-1985-455B-8825-F0987DEB8113
Q30165499-9201187A-1985-455B-8825-F0987DEB8113
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Statement
http://www.wikidata.org/entity/statement/Q30165499-9201187A-1985-455B-8825-F0987DEB8113
Non-syndromic X-linked mental retardation associated with a missense mutation (P312L) in the FGD1 gene.
P2860
Q30165499-9201187A-1985-455B-8825-F0987DEB8113
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30165499-9201187A-1985-455B-8825-F0987DEB8113
rank
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wasDerivedFrom
617e6d8ec3a218540dca6bdf35cbd883f268a6a7
P2860
Rapid immunoblot and kinase assay tests for a syndromal form of X linked mental retardation: Coffin-Lowry syndrome