Population
5 members of a family across three generations with an autosomal-dominantly inherited nondystrophic myotonic…
Design
Case_series
Authors
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Expands nondystrophic myotonia phenotypes; leaves open its genetic basis and requires confirmation in additional families.
Describes a distinct autosomal-dominant nondystrophic myotonic disorder characterized by exercise-induced delayed-onset myotonia and normal chloride conductance.
Ricker et al. (1990) studied this question.
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