Adult-Onset Fatal Neurohepatopathy in a Woman Caused by MPV17 Mutation

Hepatocerebral mitochondrial DNA depletion syndromes are classically considered diseases of early childhood, typically affecting the liver, peripheral, and central nervous systems with a rapidly progressive course. Evidence is emerging that initial symptom onset can extend into adulthood, though few...

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Main Authors: Mendelsohn, Bryce A., Mehta, Neil, Hameed, Bilal, Pekmezci, Melike, Packman, Seymour, Ralph, Jeffrey
Formato: Artigo
Idioma:Inglês
Publicado: Springer Berlin Heidelberg 2013
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Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC4110326/
https://ncbi.nlm.nih.gov/pubmed/24190800
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/8904_2013_267
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