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Q36591206-67B1A3A5-74AB-4228-9471-EC97B6714059
Q36591206-67B1A3A5-74AB-4228-9471-EC97B6714059
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http://www.wikidata.org/entity/statement/Q36591206-67B1A3A5-74AB-4228-9471-EC97B6714059
Xp11.2 microduplications including IQSEC2, TSPYL2 and KDM5C genes in patients with neurodevelopmental disorders.
P2860
Q36591206-67B1A3A5-74AB-4228-9471-EC97B6714059
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36591206-67B1A3A5-74AB-4228-9471-EC97B6714059
rank
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type
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wasDerivedFrom
062ac0e15b0f3943d899f49fa6c7404410df8c26
P2860
A noncoding, regulatory mutation implicates HCFC1 in nonsyndromic intellectual disability