Literature DB >> 2566813

Mitochondrial complex I deficiency in Parkinson's disease.

A H Schapira, J M Cooper, D Dexter, P Jenner, J B Clark, C D Marsden.   

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Year:  1989        PMID: 2566813     DOI: 10.1016/s0140-6736(89)92366-0

Source DB:  PubMed          Journal:  Lancet        ISSN: 0140-6736            Impact factor:   79.321


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  426 in total

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Review 7.  The genetic basis of Parkinson's disease.

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9.  Mitochondrial permeability transition pore regulates Parkinson's disease development in mutant α-synuclein transgenic mice.

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