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Q51010632-43C1470E-AE82-446E-8898-95A2189512A8
Q51010632-43C1470E-AE82-446E-8898-95A2189512A8
BestRank
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http://www.wikidata.org/entity/statement/Q51010632-43C1470E-AE82-446E-8898-95A2189512A8
Whole exome sequencing and functional studies identify an intronic mutation in TRAPPC2 that causes SEDT.
P2860
Q51010632-43C1470E-AE82-446E-8898-95A2189512A8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51010632-43C1470E-AE82-446E-8898-95A2189512A8
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wasDerivedFrom
099e7659d309bc6a57266a9d7f91198b1e602b1d
P2860
An analysis of exome sequencing for diagnostic testing of the genes associated with muscle disease and spastic paraplegia.