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Q48943899-BEE9457B-EE1C-4C28-89CD-C4744F554868
Q48943899-BEE9457B-EE1C-4C28-89CD-C4744F554868
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http://www.wikidata.org/entity/statement/Q48943899-BEE9457B-EE1C-4C28-89CD-C4744F554868
Properties of human glycine receptors containing the hyperekplexia mutation alpha1(K276E), expressed in Xenopus oocytes.
P2860
Q48943899-BEE9457B-EE1C-4C28-89CD-C4744F554868
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48943899-BEE9457B-EE1C-4C28-89CD-C4744F554868
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wasDerivedFrom
664d3f5bd807223edc2098148ad5aa2ab6cbbec8
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