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Q36292736-0F4C2A8D-12FA-4993-9D7B-9C70B7B0310F
Q36292736-0F4C2A8D-12FA-4993-9D7B-9C70B7B0310F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36292736-0F4C2A8D-12FA-4993-9D7B-9C70B7B0310F
Next generation sequencing in a large cohort of patients presenting with neuromuscular disease before or at birth
P2860
Q36292736-0F4C2A8D-12FA-4993-9D7B-9C70B7B0310F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36292736-0F4C2A8D-12FA-4993-9D7B-9C70B7B0310F
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Statement
wasDerivedFrom
17cc0fc3012a64dd17f5df1753644b5e467aef4b
P2860
A novel syndrome of Klippel-Feil anomaly, myopathy, and characteristic facies is linked to a null mutation in MYO18B.