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Q36695120-57E132CA-FD7E-49AA-862C-D3A2E6491798
Q36695120-57E132CA-FD7E-49AA-862C-D3A2E6491798
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36695120-57E132CA-FD7E-49AA-862C-D3A2E6491798
Loss-of-function variants of SETD5 cause intellectual disability and the core phenotype of microdeletion 3p25.3 syndrome.
P1433
Q36695120-57E132CA-FD7E-49AA-862C-D3A2E6491798
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36695120-57E132CA-FD7E-49AA-862C-D3A2E6491798
rank
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type
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wasDerivedFrom
d8af3cb9a6d5b19ce7f20b34b4d7fc22392a84e7
P1433
European Journal of Human Genetics