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Q41922212-08BAA161-B361-4FA1-A705-7D84B0E55864
Q41922212-08BAA161-B361-4FA1-A705-7D84B0E55864
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41922212-08BAA161-B361-4FA1-A705-7D84B0E55864
Loss of the arginine methyltranserase PRMT7 causes syndromic intellectual disability with microcephaly and brachydactyly.
P2860
Q41922212-08BAA161-B361-4FA1-A705-7D84B0E55864
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41922212-08BAA161-B361-4FA1-A705-7D84B0E55864
rank
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wasDerivedFrom
b7a39f77afa90460915fd1914f4d868ceb373172
P2860
The testis-specific factor CTCFL cooperates with the protein methyltransferase PRMT7 in H19 imprinting control region methylation