MICM By PCR Maternally Inherited Cardiomyopathy
This molecular test uses polymerase chain reaction (PCR) to detect mitochondrial DNA mutations associated with maternally inherited cardiomyopathy. It supports diagnosis in patients with unexplained cardiomyopathy, muscle weakness, or family history suggestive of mitochondrial disease. The test assists in genetic counseling and risk assessment of maternal relatives.
MICM By PCR Maternally Inherited Cardiomyopathy
MICM By PCR Maternally Inherited Cardiomyopathy
