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Q52639570-554947EA-1ED9-4903-ACC4-446B1C47AB88
Q52639570-554947EA-1ED9-4903-ACC4-446B1C47AB88
BestRank
Statement
http://www.wikidata.org/entity/statement/Q52639570-554947EA-1ED9-4903-ACC4-446B1C47AB88
A novel variant in MED12 gene: Further delineation of phenotype.
P2860
Q52639570-554947EA-1ED9-4903-ACC4-446B1C47AB88
BestRank
Statement
http://www.wikidata.org/entity/statement/Q52639570-554947EA-1ED9-4903-ACC4-446B1C47AB88
rank
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type
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wasDerivedFrom
940d9a1839783b6c3005ee9c59b10d76f4ccb435
P2860
Mutations in MED12 cause X-linked Ohdo syndrome