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Q24676257-F3EEC7AE-C23B-4DF2-8FD8-9BE3A5D19F09
Q24676257-F3EEC7AE-C23B-4DF2-8FD8-9BE3A5D19F09
BestRank
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http://www.wikidata.org/entity/statement/Q24676257-F3EEC7AE-C23B-4DF2-8FD8-9BE3A5D19F09
A GLRA1 null mutation in recessive hyperekplexia challenges the functional role of glycine receptors
P2860
Q24676257-F3EEC7AE-C23B-4DF2-8FD8-9BE3A5D19F09
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24676257-F3EEC7AE-C23B-4DF2-8FD8-9BE3A5D19F09
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wasDerivedFrom
112a809f605382c284c1f8aadd1d2e84c0e3c968
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