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Q47751690-EC2B0A2F-B0ED-47D2-AF24-8C5A8F3F6CE7
Q47751690-EC2B0A2F-B0ED-47D2-AF24-8C5A8F3F6CE7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47751690-EC2B0A2F-B0ED-47D2-AF24-8C5A8F3F6CE7
Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families.
P2860
Q47751690-EC2B0A2F-B0ED-47D2-AF24-8C5A8F3F6CE7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47751690-EC2B0A2F-B0ED-47D2-AF24-8C5A8F3F6CE7
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Statement
wasDerivedFrom
192aa372bf11c044d397b65d84fa10e87f42b297
P2860
Heterozygous Mutations in MAP3K7, Encoding TGF-β-Activated Kinase 1, Cause Cardiospondylocarpofacial Syndrome.