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Q36516769-4D97C0E1-D043-43EB-959F-BC3CB30663B7
Q36516769-4D97C0E1-D043-43EB-959F-BC3CB30663B7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36516769-4D97C0E1-D043-43EB-959F-BC3CB30663B7
A recessive Nav1.4 mutation underlies congenital myasthenic syndrome with periodic paralysis.
P2860
Q36516769-4D97C0E1-D043-43EB-959F-BC3CB30663B7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36516769-4D97C0E1-D043-43EB-959F-BC3CB30663B7
rank
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type
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Statement
wasDerivedFrom
0a382eb17dd4736a4e9aa49f671227e800f8ae1a
P2860
Characterization of a new sodium channel mutation at arginine 1448 associated with moderate Paramyotonia congenita in humans