(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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scholarly article

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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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Werner syndrome

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author name string

M. Lebel

1

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language of work or name

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publication date

1 June 2001

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Cellular and Molecular Life Sciences

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58

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7

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857-867

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https://scigraph.springernature.com/pub.10.1007/s00018-001-8398-y

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Identifiers

10.1007/S00018-001-8398-Y

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