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Q47665402-86371A29-2725-4141-9E92-F9B853AFA620
Q47665402-86371A29-2725-4141-9E92-F9B853AFA620
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47665402-86371A29-2725-4141-9E92-F9B853AFA620
Heterozygous mutations affecting the protein kinase domain of CDK13 cause a syndromic form of developmental delay and intellectual disability.
P2860
Q47665402-86371A29-2725-4141-9E92-F9B853AFA620
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47665402-86371A29-2725-4141-9E92-F9B853AFA620
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wasDerivedFrom
d4f5ccb9b79ef668a720c5a96e21f99d375e7146
P2860
Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing.