Specific correlation between the wobble modification deficiency in mutant tRNAs and the clinical features of a human mitochondrial disease

  1. Kirino, Y.
  2. Goto, Y.-I.
  3. Campos, Y.
  4. Arenas, J.
  5. Suzuki, T.
Aldizkaria:
Proceedings of the National Academy of Sciences of the United States of America

ISSN: 0027-8424

Argitalpen urtea: 2005

Alea: 102

Zenbakia: 20

Orrialdeak: 7127-7132

Mota: Artikulua

DOI: 10.1073/PNAS.0500563102 GOOGLE SCHOLAR lock_openSarbide irekia editor
Datuen iturria: Scopus