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Q50626990-3B480DBE-D53F-4F97-91B6-19104B315DF6
Q50626990-3B480DBE-D53F-4F97-91B6-19104B315DF6
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http://www.wikidata.org/entity/statement/Q50626990-3B480DBE-D53F-4F97-91B6-19104B315DF6
Compound heterozygous mutations in RIPPLY2 associated with vertebral segmentation defects.
P2860
Q50626990-3B480DBE-D53F-4F97-91B6-19104B315DF6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q50626990-3B480DBE-D53F-4F97-91B6-19104B315DF6
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wasDerivedFrom
fe0691cda66a6cfa8c15e794d2e6c84692b37d8b
P2860
Mutations in MEOX1, encoding mesenchyme homeobox 1, cause Klippel-Feil anomaly.