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Q41928481-7853CD51-A662-467A-A2E2-095420744529
Q41928481-7853CD51-A662-467A-A2E2-095420744529
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41928481-7853CD51-A662-467A-A2E2-095420744529
A novel syndrome of Klippel-Feil anomaly, myopathy, and characteristic facies is linked to a null mutation in MYO18B.
P2860
Q41928481-7853CD51-A662-467A-A2E2-095420744529
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41928481-7853CD51-A662-467A-A2E2-095420744529
rank
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type
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Statement
wasDerivedFrom
d2c75167dcd80bf27ce1c5126d1b4ec100be42d5
P2860
Autosomal dominant myopathy: missense mutation (Glu-706 --> Lys) in the myosin heavy chain IIa gene