The effect of LMNA mutations on the lamin IG-fold structure and muscle gene expression

Mutations in the human LMNA gene encoding A-type lamins cause a collection of diseases termed laminopathies, including several types of muscular dystrophy. Lamins are intermediate filaments, which line the inner membrane of nuclear envelope. Lamins maintain the nuclear shape and regulate gene expres...

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Bibliographic Details
Main Author: Shrestha, Om Kumar
Other Authors: Wallrath, Lori L.
Format: Others
Language:English
Published: University of Iowa 2012
Subjects:
NMR
Online Access:https://ir.uiowa.edu/etd/3383
https://ir.uiowa.edu/cgi/viewcontent.cgi?article=3328&context=etd