Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Abdeldjalil Boucheham"'
Autor:
Abdeldjalil Boucheham, Anne-Marie Mager-Heckel, Tom Schirtz, Olga Karicheva, Robert P. Martin, Nina Entelis, Olga Kolesnikova, Mikhail Y. Vysokikh, Igor A. Krasheninnikov, Anne Lombès, Ivan Tarassov
Publikováno v:
Nucleic Acids Research
Mutations in human mitochondrial DNA are often associated with incurable human neuromuscular diseases. Among these mutations, an important number have been identified in tRNA genes, including 29 in the gene MT-TL1 coding for the tRNA(Leu(UUR)). The m
Autor:
Nina Entelis, Yann Tonin, Alexandre Smirnov, Ivan Tarassov, Karine Auré, Anne Lombès, Abdeldjalil Boucheham, Caroline Comte, Robert P. Martin, Anne-Marie Heckel-Mager
Publikováno v:
Nucleic Acids Research
Nucleic Acids Research, 2013, 41 (1), pp.418-433. ⟨10.1093/nar/gks965⟩
Nucleic Acids Research, Oxford University Press, 2013, 41 (1), pp.418-433. ⟨10.1093/nar/gks965⟩
Nucleic Acids Research, 2013, 41 (1), pp.418-433. ⟨10.1093/nar/gks965⟩
Nucleic Acids Research, Oxford University Press, 2013, 41 (1), pp.418-433. ⟨10.1093/nar/gks965⟩
International audience; Mitochondrial mutations, an important cause of incurable human neuromuscular diseases, are mostly heteroplasmic: mutated mitochondrial DNA is present in cells simultaneously with wild-type genomes, the pathogenic threshold bei
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e50a0b2e208d144f39663197b4504dc
https://hal.sorbonne-universite.fr/hal-01587401/document
https://hal.sorbonne-universite.fr/hal-01587401/document