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High-dose thiamine prevents brain lesions and prolongs survival of Slc19a3-deficient mice
SLC19A3 deficiency, also called thiamine metabolism dysfunction syndrome-2 (THMD2; OMIM 607483), is an autosomal recessive neurodegenerative disorder caused by mutations in SLC19A3, the gene encoding thiamine transporter 2. To investigate the molecular mechanisms of neurodegeneration in SLC19A3 defi...
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| Publicado en: | PLoS One |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Public Library of Science
2017
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5493381/ https://ncbi.nlm.nih.gov/pubmed/28665968 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0180279 |
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