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Q28118429-3058608E-1CA5-4AF0-B710-08E9D4A20413
Q28118429-3058608E-1CA5-4AF0-B710-08E9D4A20413
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Statement
http://www.wikidata.org/entity/statement/Q28118429-3058608E-1CA5-4AF0-B710-08E9D4A20413
A human laterality disorder caused by a homozygous deleterious mutation in MMP21
P2860
Q28118429-3058608E-1CA5-4AF0-B710-08E9D4A20413
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28118429-3058608E-1CA5-4AF0-B710-08E9D4A20413
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wasDerivedFrom
d7772afee31f7fe4e2fea7e7d9526a2480b4db59
P2860
Reduced NODAL signaling strength via mutation of several pathway members including FOXH1 is linked to human heart defects and holoprosencephaly