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Q30450702-4EB7698A-4C49-48C2-9F32-847A6F7BC0E8
Q30450702-4EB7698A-4C49-48C2-9F32-847A6F7BC0E8
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Statement
http://www.wikidata.org/entity/statement/Q30450702-4EB7698A-4C49-48C2-9F32-847A6F7BC0E8
Mutations in the GlyT2 gene (SLC6A5) are a second major cause of startle disease.
P2860
Q30450702-4EB7698A-4C49-48C2-9F32-847A6F7BC0E8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30450702-4EB7698A-4C49-48C2-9F32-847A6F7BC0E8
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wasDerivedFrom
cffe51de1a240acdbc807b66f1b856ceb7b6bef3
P2860
Startle disease in Irish wolfhounds associated with a microdeletion in the glycine transporter GlyT2 gene.