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Q34969098-FBA7CF52-ED43-40DE-93A3-CA5F10178117
Q34969098-FBA7CF52-ED43-40DE-93A3-CA5F10178117
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34969098-FBA7CF52-ED43-40DE-93A3-CA5F10178117
Novel phenotype associated with a mutation in the KCNA1(Kv1.1) gene
P2860
Q34969098-FBA7CF52-ED43-40DE-93A3-CA5F10178117
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34969098-FBA7CF52-ED43-40DE-93A3-CA5F10178117
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wasDerivedFrom
1c00e06f144342ad4cd8519321faab93c0f916e9
P2860
Expanding the phenotype of potassium channelopathy: severe neuromyotonia and skeletal deformities without prominent Episodic Ataxia