Structure and stability of the lamin A tail domain and HGPS mutant
Hutchinson–Gilford progeria syndrome (HGPS) is a premature aging syndrome caused by the expression and accumulation of a mutant form of lamin A, Δ50 lamin A. As a component of the cell’s nucleoskeleton, lamin A plays an important role in the mechanical stabilization of the nuclear envelope and in ot...
| Main Authors: | , , , |
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| Other Authors: | |
| Format: | Article |
| Language: | en_US |
| Published: |
Elsevier
2015
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| Online Access: | http://hdl.handle.net/1721.1/99226 https://orcid.org/0000-0002-4173-9659 |