X. A. Tran

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  • Nipavan Cortopassi, Donald M Chiamvimonvat, Marcela Bers, Anne A Votruba, Le Knowlton, Tingting Chen +16 others
  • 2012
Background-—Mitochondrial fusion protein mutations are a cause of inherited neuropathies such as Charcot–Marie–Tooth disease and dominant optic atrophy. Previously we reported that the fusion protein optic atrophy 1 (OPA1) is decreased in heart failure.
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