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...
Main Authors: | , , , |
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Other Authors: | , , |
Format: | Article |
Language: | English |
Published: |
Elsevier,
2015-10-13T17:58:26Z.
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Subjects: | |
Online Access: | Get fulltext |