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Congenital Myopathy 16
A congenital myopathy that is characterized by onset of hypotonia and tremor in infancy and that is caused by heterozygous mutation in the MYBPC1 gene on chromosome 12q23. Patients have mildly delayed walking, unsteady g
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Overview
A congenital myopathy that is characterized by onset of hypotonia and tremor in infancy and that is caused by heterozygous mutation in the MYBPC1 gene on chromosome 12q23. Patients have mildly delayed walking, unsteady g
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