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Summary Literature (1)
MIM:168300 - PARAMYOTONIA CONGENITA OF VON EULENBURG; PMC

Xenbase Genes: scn4a

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008195 - paramyotonia congenita of Von Eulenburg

Disease Ontology (DO):
DOID:0111538 - paramyotonia congenita of Von Eulenburg