Title : SCN4A mutation as modifying factor of myotonic dystrophy type 2 phenotype.

Pub. Date : 2015 Apr

PMID : 25660391






1 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 No DM2 cases have been described with sodium channel gene (SCN4A) mutations. Sodium sodium voltage-gated channel alpha subunit 4 Homo sapiens