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The zebrafish orthologue of the human hepatocerebral disease gene MPV17 plays pleiotropic roles in mitochondria

Mitochondrial DNA depletion syndromes (MDS) are a group of rare autosomal recessive disorders with early onset and no cure available. MDS are caused by mutations in nuclear genes involved in mitochondrial DNA (mtDNA) maintenance, and characterized by both a strong reduction in mtDNA content and seve...

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Detalhes bibliográficos
Publicado no:Dis Model Mech
Main Authors: Martorano, Laura, Peron, Margherita, Laquatra, Claudio, Lidron, Elisa, Facchinello, Nicola, Meneghetti, Giacomo, Tiso, Natascia, Rasola, Andrea, Ghezzi, Daniele, Argenton, Francesco
Formato: Artigo
Idioma:Inglês
Publicado em: The Company of Biologists Ltd 2019
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6451431/
https://ncbi.nlm.nih.gov/pubmed/30833296
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dmm.037226
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