Bilateral Striatal Necrosis and MELAS Associated with a New T3308C Mutation in the Mitochondrial ND1 Gene
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference9 articles.
1. MOLECULAR GENETIC ASPECTS OF HUMAN MITOCHONDRIAL DISORDERS
2. Mitochondrial Encephalomyopathies
3. A new mutation associated with MELAS is located in a mitochondrial DNA polypeptide-coding gene
4. Mitochondrial DNA deletion in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes (MELAS) and Fanconi's syndrome
5. Sequence and organization of the human mitochondrial genome
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