Phenotypic heterogeneity in families with the myoclonic epilepsy and ragged‐red fiber disease point mutation in mitochondrial DNA
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S. M. Sumi | S. Dimauro | M. Copass | W. Longstreth | W. Longstreth | A. Lombès | S. Shanske | L. Ojemann | W. Graf | S. DiMauro | S. Sumi