Homoplasmic mitochondrial DNA diseases as the paradigm to understand the tissue specificity and variable clinical severity of mitochondrial disorders.

PubWeight™: 0.83^‹?›

🔗 View Article (PMID 11001802)

Published in Mol Genet Metab on November 13, 2000

Authors

N Fischel-Ghodsian¹

Author Affiliations

1: Ahmanson Department of Pediatrics, Cedars-Sinai Medical Center and UCLA School of Medicine, Los Angeles, California 90048, USA.

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