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Magnesium treatment for patients with refractory status epilepticus due to POLG1-mutations
Mutations in the gene encoding of the catalytic subunit of mtDNA polymerase gamma (POLG1) can cause typical Alpers' syndrome. Recently, a new POLG1 mutation phenotype was described, the so-called juvenile-onset Alpers' syndrome. This POLG1 mutation phenotype is characterized by refractory...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer-Verlag
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3036811/ https://ncbi.nlm.nih.gov/pubmed/20803213 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00415-010-5721-2 |
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