Population
4 patients with nonobstructive hypertrophic cardiomyopathy (HCM) from an extended Chinese family
Design
Case_series
Authors
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Alerts clinicians to fatal conduction disease in familial nonobstructive HCM; leaves open a novel genetic basis.
Describes a familial form of nonobstructive hypertrophic cardiomyopathy characterized by severe bradycardia and AV block, suggesting a potentially novel genetic mutation.
Wang et al. (2002) studied this question.
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