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Human Molecular Genetics, Vol. 17, Iss. 15, 2008-08 ,pp. : 2329-2335

Oxford University Press

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Loss of Uch-L1 and Uch-L3 leads to neurodegeneration, posterior paralysis and dysphagia

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Human Molecular Genetics, Vol. 10, Iss. 18, 2001-09 ,pp. : 1963-1970

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Thymidine kinase 2 mutations in autosomal recessive progressive external ophthalmoplegia with multiple mitochondrial DNA deletions

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An isoform of hPANK2, deficient in pantothenate kinase-associated neurodegeneration, localizes to mitochondria

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Human Molecular Genetics, Vol. 12, Iss. 3, 2003-02 ,pp. : 321-327

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Intersectin enhances huntingtin aggregation and neurodegeneration through activation of c-Jun-NH 2 -terminal kinase

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Human Molecular Genetics, Vol. 16, Iss. 15, 2007-08 ,pp. : 1862-1871

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