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Mitochondrial DNA variations in Madras motor neuron disease
Although the Madras Motor Neuron Disease (MMND) was found three decades ago, its genetic basis has not been elucidated, so far. The symptom at onset was impaired hearing, upper limb weakness and atrophy. Since some clinical features of MMND overlap with mitochondrial disorders, we analyzed the compl...
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| Publicado no: | Mitochondrion |
|---|---|
| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4805120/ https://ncbi.nlm.nih.gov/pubmed/23419391 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.mito.2013.02.003 |
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