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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Publicat a:Mitochondrion
Autors principals: Govindaraj, Periyasamy, Nalini, Atchayaram, Krishna, Nithin, Sharath, Anugula, Khan, Nahid Akhtar, Tamang, Rakesh, Devi, M. Gourie, Brown, Robert H., Thangaraj, Kumarasamy
Format: Artigo
Idioma:Inglês
Publicat: 2013
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Article
Accés en línia: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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