Mutations in MTFMT underlie a human disorder of formylation causing impaired mitochondrial translation
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S. Carr | V. Mootha | S. Dimauro | S. Calvo | J. Christodoulou | Jinal Patel | J. Jaffe | A. Compton | M. Ryan | D. Thorburn | O. Goldberger | C. Koehrer | U. RajBhandary | E. Tucker | S. Hershman | C. A. Belcher-Timme | J. M. Silberstein | M. McKenzie | C. Garone | B. García-Díaz