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Q47665402-B5574CB8-66F9-4578-AC2B-AB652E59E5BE
Q47665402-B5574CB8-66F9-4578-AC2B-AB652E59E5BE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47665402-B5574CB8-66F9-4578-AC2B-AB652E59E5BE
Heterozygous mutations affecting the protein kinase domain of CDK13 cause a syndromic form of developmental delay and intellectual disability.
P2860
Q47665402-B5574CB8-66F9-4578-AC2B-AB652E59E5BE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47665402-B5574CB8-66F9-4578-AC2B-AB652E59E5BE
rank
NormalRank
type
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Statement
wasDerivedFrom
7a0ce52ed5935d5fd0f95e8be9dc8fc1996a1c06
P2860
Mutations in MED12 cause X-linked Ohdo syndrome