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Q34160063-4616EF82-7F10-49B6-9633-3FB5CFF03753
Q34160063-4616EF82-7F10-49B6-9633-3FB5CFF03753
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34160063-4616EF82-7F10-49B6-9633-3FB5CFF03753
Disorders with similar clinical phenotypes reveal underlying genetic interaction: SATB2 acts as an activator of the UPF3B gene.
P2860
Q34160063-4616EF82-7F10-49B6-9633-3FB5CFF03753
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34160063-4616EF82-7F10-49B6-9633-3FB5CFF03753
rank
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type
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Statement
wasDerivedFrom
f35ce289115673159db901659d59bcaf310196bb
P2860
Heterozygous nonsense mutation SATB2 associated with cleft palate, osteoporosis, and cognitive defects.