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Lamin A Truncation in Hutchinson-Gilford Progeria
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Mutations in genes encoding protein components of the nuclear lamina, or factors affecting their maturation and dynamics, cause accelerated aging syndromes such as Hutchinson-Gilford and Néstor-Guillermo progeria syndromes.
“The nuclear lamina attracted the attention of aging researchers after the discovery that mutations in genes encoding protein components of this structure, or factors affecting their maturation and dynamics, cause accelerated aging syndromes such as the Hutchinson-Gilford and the Néstor-Guillermo progeria syndromes (HGPS and NGPS, respectively) (Cabanillas et al., 2011; De Sandre-Giovannoli et al.,”
From The Hallmarks of Aging (2013) · cites this paper as De Sandre-Giovannoli et al., 2003
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Metadata
- Authors
- De Sandre-Giovannoli, A., Bernard, R., Cau, P., Navarro, C., Amiel, J., Boccaccio, I., Lyonnet, S., Stewart, C. L., Munnich, A., Le Merrer, M., & Lévy, N.
- Affiliations
- Inserm U491: «Génétique Médicale et Développement», Faculté de Médecine Timone, Marseille, France.
- Venue
- Science
- Published
- 2003-06-27
- Volume
- 300
- Issue
- 5628
- Pages
- 2055-2055
- ISSN
- 0036-8075
- 1095-9203
- Cited by
- 1,346
- References
- 0
- Language
- en
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