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Primary dilated cardiomyopathy
- ... FDC Primary familial dilated cardiomyopathy Genetic Testing Registry: Primary dilated cardiomyopathy Cardiomyopathy, dilated, 1a Cardiomyopathy, dilated, 1e Dilated cardiomyopathy ...
- ... How do mutations in contractile proteins cause the primary familial cardiomyopathies? J Cardiovasc Transl Res. 2011 Jun;4(3): ...
- ... How do mutations in contractile proteins cause the primary familial cardiomyopathies? J Cardiovasc Transl Res. 2011 Jun;4(3): ...
- ... How do mutations in contractile proteins cause the primary familial cardiomyopathies? J Cardiovasc Transl Res. 2011 Jun;4(3): ...
- ... How do mutations in contractile proteins cause the primary familial cardiomyopathies? J Cardiovasc Transl Res. 2011 Jun;4(3): ...
- ... Bonilla E, Nonaka I, DiMauro S, Hirano M. Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease). Nature. 2000 Aug 24; ...
- ... that enlarges and weakens the heart muscle (hypertrophic cardiomyopathy) can also occur in primary coenzyme Q10 deficiency. The prevalence of primary coenzyme ...
- ... fats and produce energy.Signs and symptoms of primary carnitine deficiency typically appear during infancy or early childhood and can include severe brain dysfunction (encephalopathy), a weakened and enlarged heart (cardiomyopathy), vomiting, muscle weakness, and low blood glucose (hypoglycemia). ...
- ... begin anytime from infancy to adulthood, is the primary symptom. The liver ... (cardiomyopathy). Other features of this condition include excess ammonia ...
- ... This Health Condition MedlinePlus Genetics provides information about Primary myelofibrosis More About This Health Condition Somatic mutations ... been associated with other forms of cancer, including primary myelofibrosis (linked above) and brain tumors called gliomas. ...
