Histochemical and Molecular Genetic Study of MELAS and MERRF in Korean Patients
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چکیده
منابع مشابه
Histochemical and molecular genetic study of MELAS and MERRF in Korean patients.
Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episode (MELAS) and myoclonic epilepsy and ragged-red fibers (MERRF) are rare disorders caused by point mutation of the tRNA gene of the mitochondrial genome. To understand the pathogenetic mechanism of MELAS and MERRF, we studied four patients. Serially sectioned frozen muscle specimens with a battery of histochemical stai...
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ژورنال
عنوان ژورنال: Journal of Korean Medical Science
سال: 2002
ISSN: 1011-8934,1598-6357
DOI: 10.3346/jkms.2002.17.1.103