Molecular and Pathological Analyses of IARS1-Deficient Mice: An IARS Disorder Model

Most mitochondrial diseases are hereditary and highly heterogeneous. Cattle born with the V79L mutation in the isoleucyl-tRNA synthetase 1 (IARS1) protein exhibit weak calf syndrome. Recent human genomic studies about pediatric mitochondrial diseases also identified mutations in the IARS1 gene. Alth...

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Detalles Bibliográficos
Autores principales: Watanabe, Masaki, Shishido, Koya, Kanehira, Nao, Hiura, Koki, Nakano, Kenta, Okamura, Tadashi, Ando, Ryo, Sasaki, Hayato, Sasaki, Nobuya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10138339/
https://www.ncbi.nlm.nih.gov/pubmed/37108118
http://dx.doi.org/10.3390/ijms24086955

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10138339/
https://www.ncbi.nlm.nih.gov/pubmed/37108118
http://dx.doi.org/10.3390/ijms24086955

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