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Q41928481-0CB13C78-F8D7-49B4-A0AC-F19DFBF73F05
Q41928481-0CB13C78-F8D7-49B4-A0AC-F19DFBF73F05
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Statement
http://www.wikidata.org/entity/statement/Q41928481-0CB13C78-F8D7-49B4-A0AC-F19DFBF73F05
A novel syndrome of Klippel-Feil anomaly, myopathy, and characteristic facies is linked to a null mutation in MYO18B.
P2860
Q41928481-0CB13C78-F8D7-49B4-A0AC-F19DFBF73F05
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41928481-0CB13C78-F8D7-49B4-A0AC-F19DFBF73F05
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wasDerivedFrom
d2c75167dcd80bf27ce1c5126d1b4ec100be42d5
P2860
The concerted action of Meox homeobox genes is required upstream of genetic pathways essential for the formation, patterning and differentiation of somites