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Q24321507-C75CB005-BD65-42F8-98CE-187B00C17BD6
Q24321507-C75CB005-BD65-42F8-98CE-187B00C17BD6
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http://www.wikidata.org/entity/statement/Q24321507-C75CB005-BD65-42F8-98CE-187B00C17BD6
Functional analysis of a novel potassium channel (KCNA1) mutation in hereditary myokymia
P2860
Q24321507-C75CB005-BD65-42F8-98CE-187B00C17BD6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24321507-C75CB005-BD65-42F8-98CE-187B00C17BD6
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cb01ec08bde6be9d78fb90ee886c684c5d1b443c
P2860
Expanding the phenotype of potassium channelopathy: severe neuromyotonia and skeletal deformities without prominent Episodic Ataxia