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Q41928481-2B1970F9-A3F4-4A53-BCB8-8D7C81D40DA6
Q41928481-2B1970F9-A3F4-4A53-BCB8-8D7C81D40DA6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41928481-2B1970F9-A3F4-4A53-BCB8-8D7C81D40DA6
A novel syndrome of Klippel-Feil anomaly, myopathy, and characteristic facies is linked to a null mutation in MYO18B.
P577
Q41928481-2B1970F9-A3F4-4A53-BCB8-8D7C81D40DA6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41928481-2B1970F9-A3F4-4A53-BCB8-8D7C81D40DA6
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
0cce053421955450eec38eb32b50a8b29521bbd8
P577
2015-03-06T00:00:00Z
http://www.w3.org/2001/XMLSchema#dateTime
P577
ce7e41ae36635bd35d0cfe32cf4635b7