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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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| Asıl Yazarlar: | , , , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Springer Berlin Heidelberg
2013
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| Konular: | |
| Online Erişim: | 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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