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Q47582519-00A132FD-A3BB-43DA-ABF0-08F75071B0B1
Q47582519-00A132FD-A3BB-43DA-ABF0-08F75071B0B1
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http://www.wikidata.org/entity/statement/Q47582519-00A132FD-A3BB-43DA-ABF0-08F75071B0B1
Choline transporter mutations in severe congenital myasthenic syndrome disrupt transporter localization.
P2860
Q47582519-00A132FD-A3BB-43DA-ABF0-08F75071B0B1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47582519-00A132FD-A3BB-43DA-ABF0-08F75071B0B1
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wasDerivedFrom
848d8103d78f8c3d6eca4ce20c121cbb0dc87af2
P2860
T222P mutation of the insulin-like 3 hormone receptor LGR8 is associated with testicular maldescent and hinders receptor expression on the cell surface membrane.