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Reduced Mitochondrial DNA Content and Heterozygous Nuclear Gene Mutations in Patients with Acute Liver Failure
OBJECTIVES: Historically, mitochondrial disorders have been associated with predominantly multisystem or neurological symptoms. If present, hepatic complications were thought to be a late feature. Recently, mutations in at least 4 nuclear genes have been identified in infants presenting with rapidly...
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| Publicado no: | J Pediatr Gastroenterol Nutr |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4966813/ https://ncbi.nlm.nih.gov/pubmed/23783014 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MPG.0b013e31829ef4b4 |
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