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


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

In Mondo Disease Ontology:
MONDO:0008195 - paramyotonia congenita of Von Eulenburg

Human Disease Resources: OMIM

Xenbase Genes: scn4a