Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
6041676 | Neuromuscular Disorders | 2011 | 4 Pages |
Abstract
We describe three Belgian families with a L1436P mutation in the SCN4A gene, causing a sodium channel myotonia with an atypical clinical presentation, characterized by late onset painful cold-aggravated myotonia. These families represent a distinct phenotype within the spectrum of sodium channel myotonia.
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Authors
Véronique Bissay, Kathelijn Keymolen, Willy Lissens, Guy Laureys, Eric Schmedding, Jacques De Keyser,