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Q24602558-82DCEBFD-42AB-4A3E-B963-79F6463FCF86
Q24602558-82DCEBFD-42AB-4A3E-B963-79F6463FCF86
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http://www.wikidata.org/entity/statement/Q24602558-82DCEBFD-42AB-4A3E-B963-79F6463FCF86
Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1.
P2860
Q24602558-82DCEBFD-42AB-4A3E-B963-79F6463FCF86
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24602558-82DCEBFD-42AB-4A3E-B963-79F6463FCF86
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wasDerivedFrom
d6e23f847e43d61b6ccdb7e832ec5eeecf6bf32c
P2860
Rare copy number variants are an important cause of epileptic encephalopathies.