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Q41928481-C494D809-FED2-4E22-B785-921FB655BF18
Q41928481-C494D809-FED2-4E22-B785-921FB655BF18
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41928481-C494D809-FED2-4E22-B785-921FB655BF18
A novel syndrome of Klippel-Feil anomaly, myopathy, and characteristic facies is linked to a null mutation in MYO18B.
P31
Q41928481-C494D809-FED2-4E22-B785-921FB655BF18
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41928481-C494D809-FED2-4E22-B785-921FB655BF18
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
0cce053421955450eec38eb32b50a8b29521bbd8
P31
scholarly article