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Q47229502-DD41053A-5A67-4CB5-99CB-A970C5FCB217
Q47229502-DD41053A-5A67-4CB5-99CB-A970C5FCB217
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http://www.wikidata.org/entity/statement/Q47229502-DD41053A-5A67-4CB5-99CB-A970C5FCB217
Regulatory variants of FOXG1 in the context of its topological domain organisation.
P2860
Q47229502-DD41053A-5A67-4CB5-99CB-A970C5FCB217
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47229502-DD41053A-5A67-4CB5-99CB-A970C5FCB217
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wasDerivedFrom
fc782af428d3a5285925e45b9b2d9ec720da0be4
P2860
14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotype.