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Q30481905-AE4D78FB-CEFF-4A39-8D1A-C14473756CB8
Q30481905-AE4D78FB-CEFF-4A39-8D1A-C14473756CB8
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http://www.wikidata.org/entity/statement/Q30481905-AE4D78FB-CEFF-4A39-8D1A-C14473756CB8
The glycinergic system in human startle disease: a genetic screening approach.
P2860
Q30481905-AE4D78FB-CEFF-4A39-8D1A-C14473756CB8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30481905-AE4D78FB-CEFF-4A39-8D1A-C14473756CB8
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wasDerivedFrom
24bd5f1a488e2d7a91b6843c2bf5dddbf3bf5463
P2860
Evidence for recessive as well as dominant forms of startle disease (hyperekplexia) caused by mutations in the alpha 1 subunit of the inhibitory glycine receptor