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Q37671232-03D86D28-4CAD-409D-9D73-A1164C41F8A0
Q37671232-03D86D28-4CAD-409D-9D73-A1164C41F8A0
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http://www.wikidata.org/entity/statement/Q37671232-03D86D28-4CAD-409D-9D73-A1164C41F8A0
Electrophysiological characteristics of six mutations in hClC-1 of Korean patients with myotonia congenita.
P2860
Q37671232-03D86D28-4CAD-409D-9D73-A1164C41F8A0
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Statement
http://www.wikidata.org/entity/statement/Q37671232-03D86D28-4CAD-409D-9D73-A1164C41F8A0
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926013fe0cde223224da7d4dfadbf546bdebd705
P2860
A mutation in autosomal dominant myotonia congenita affects pore properties of the muscle chloride channel