Article ID Journal Published Year Pages File Type
6041676 Neuromuscular Disorders 2011 4 Pages PDF
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.
Related Topics
Life Sciences Neuroscience Developmental Neuroscience
Authors
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