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Q37589691-FE2F2F91-EB18-4317-AB9A-459C96D17AB5
Q37589691-FE2F2F91-EB18-4317-AB9A-459C96D17AB5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37589691-FE2F2F91-EB18-4317-AB9A-459C96D17AB5
A Premature Stop Codon in MYO18B is Associated with Severe Nemaline Myopathy with Cardiomyopathy.
P2860
Q37589691-FE2F2F91-EB18-4317-AB9A-459C96D17AB5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37589691-FE2F2F91-EB18-4317-AB9A-459C96D17AB5
rank
NormalRank
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Statement
wasDerivedFrom
c81ccceb4f5fc7e682f72b18e26b15d22c3451fb
P2860
A novel syndrome of Klippel-Feil anomaly, myopathy, and characteristic facies is linked to a null mutation in MYO18B.