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Q43663646-5A1B887A-EA8F-41D2-90B7-1E9C8C53C1AF
Q43663646-5A1B887A-EA8F-41D2-90B7-1E9C8C53C1AF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q43663646-5A1B887A-EA8F-41D2-90B7-1E9C8C53C1AF
Novel PRRT2 mutations in paroxysmal dyskinesia patients with variant inheritance and phenotypes.
P2860
Q43663646-5A1B887A-EA8F-41D2-90B7-1E9C8C53C1AF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q43663646-5A1B887A-EA8F-41D2-90B7-1E9C8C53C1AF
rank
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wasDerivedFrom
3c079abe2111ba24410d0a2ff6e028595068bee2
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