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Q41075733-17738CEA-5621-4398-95EC-CF2CEF73644C
Q41075733-17738CEA-5621-4398-95EC-CF2CEF73644C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41075733-17738CEA-5621-4398-95EC-CF2CEF73644C
Clinical application of whole-exome sequencing across clinical indications.
P2860
Q41075733-17738CEA-5621-4398-95EC-CF2CEF73644C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41075733-17738CEA-5621-4398-95EC-CF2CEF73644C
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379816ed3c487949eca53bae14aa17e5d4817943
P2860
Dominant mutations in KAT6A cause intellectual disability with recognizable syndromic features.