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Q34649239-68B74EF0-5198-43CA-8500-2868E3C7B17C
Q34649239-68B74EF0-5198-43CA-8500-2868E3C7B17C
BestRank
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http://www.wikidata.org/entity/statement/Q34649239-68B74EF0-5198-43CA-8500-2868E3C7B17C
The neuronal channelopathies.
P2860
Q34649239-68B74EF0-5198-43CA-8500-2868E3C7B17C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34649239-68B74EF0-5198-43CA-8500-2868E3C7B17C
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wasDerivedFrom
4823e89eedbcd1a781e371c12b61b2dd55c129cb
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