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Q41929209-75961865-6436-47D8-B9D3-769BC332FF64
Q41929209-75961865-6436-47D8-B9D3-769BC332FF64
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41929209-75961865-6436-47D8-B9D3-769BC332FF64
De novo mutations in beta-catenin (CTNNB1) appear to be a frequent cause of intellectual disability: expanding the mutational and clinical spectrum.
P2860
Q41929209-75961865-6436-47D8-B9D3-769BC332FF64
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41929209-75961865-6436-47D8-B9D3-769BC332FF64
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wasDerivedFrom
5c05fc706c5276cb9c81b4ed27195679fa59ae9b
P2860
Loss-of-function variants of SETD5 cause intellectual disability and the core phenotype of microdeletion 3p25.3 syndrome.