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Q35924886-DD2A7600-2E5B-40EA-8BE8-A59F5B285349
Q35924886-DD2A7600-2E5B-40EA-8BE8-A59F5B285349
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Statement
http://www.wikidata.org/entity/statement/Q35924886-DD2A7600-2E5B-40EA-8BE8-A59F5B285349
Nonsyndromic X-linked intellectual deficiency in three brothers with a novel MED12 missense mutation [c.5922G>T (p.Glu1974His)].
P2860
Q35924886-DD2A7600-2E5B-40EA-8BE8-A59F5B285349
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35924886-DD2A7600-2E5B-40EA-8BE8-A59F5B285349
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Statement
wasDerivedFrom
5171dfe4a3011413e85d2e975003035181cc2155
P2860
Mutations in MED12 cause X-linked Ohdo syndrome