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Q35546508-EA841B27-DD46-49AE-BC9E-C068A6C75932
Q35546508-EA841B27-DD46-49AE-BC9E-C068A6C75932
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http://www.wikidata.org/entity/statement/Q35546508-EA841B27-DD46-49AE-BC9E-C068A6C75932
PHF6 Deletions May Cause Borjeson-Forssman-Lehmann Syndrome in Females.
P2860
Q35546508-EA841B27-DD46-49AE-BC9E-C068A6C75932
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35546508-EA841B27-DD46-49AE-BC9E-C068A6C75932
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wasDerivedFrom
645865e42f0c32cd2d0cc10534f33c76fa0c0d14
P2860
1024C> T (R342X) is a recurrent PHF6 mutation also found in the original Börjeson-Forssman-Lehmann syndrome family.