(Q56552029)

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Human Genome and Diseases: A new series of reviews in CMLS Werner Syndrome: genetic and molecular basis of a premature aging disorder

article published in 2001

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Human Genome and Diseases: A new series of reviews in CMLS Werner Syndrome: genetic and molecular basis of a premature aging disorder (English)

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M. Lebel

1

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1 June 2001

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published in

Cellular and Molecular Life Sciences

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volume

58

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issue

7

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page(s)

857-867

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10.1007/S00018-001-8398-Y

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ResearchGate publication ID

238464742

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(Q56552029)

Human Genome and Diseases: A new series of reviews in CMLS Werner Syndrome: genetic and molecular basis of a premature aging disorder

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