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1
Q53212278-F95BAFCC-93B0-4BC0-A12E-B6EA0A1A3A0C
Q53212278-F95BAFCC-93B0-4BC0-A12E-B6EA0A1A3A0C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q53212278-F95BAFCC-93B0-4BC0-A12E-B6EA0A1A3A0C
De novo, heterozygous, loss-of-function mutations in SYNGAP1 cause a syndromic form of intellectual disability.
P407
Q53212278-F95BAFCC-93B0-4BC0-A12E-B6EA0A1A3A0C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q53212278-F95BAFCC-93B0-4BC0-A12E-B6EA0A1A3A0C
rank
NormalRank
type
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Statement
P407
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