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Human Molecular Genetics, Vol. 17, Iss. 23, 2008-12 ,pp. : 3822-3835

Oxford University Press

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CAG repeat length in RAI1 is associated with age at onset variability in spinocerebellar ataxia type 2 (SCA2)

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Human Molecular Genetics, Vol. 9, Iss. 12, 2000-07 ,pp. : 1753-1758

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Similarities between spinocerebellar ataxia type 7 (SCA7) cell models and human brain: proteins recruited in inclusions and activation of caspase-3

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Human Molecular Genetics, Vol. 10, Iss. 22, 2001-10 ,pp. : 2569-2579

Oxford University Press

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Biochemical analysis of mutations in palmitoyl-protein thioesterase causing infantile and late-onset forms of neuronal ceroid lipofuscinosis

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New mouse models for recessive retinitis pigmentosa caused by mutations in the Pde6a gene

By Sakamoto Kenji   McCluskey Michael   Wensel Theodore G.   Naggert Jrgen K.   Nishina Patsy M.  

Human Molecular Genetics, Vol. 18, Iss. 1, 2009-01 ,pp. : 178-192

Oxford University Press

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