Lamin A and lamin C are differentially dysfunctional in autosomal dominant Emery-Dreifuss muscular dystrophy
Emery-Dreifuss muscular dystrophy (EDMD) is a rare genetic disorder characterised by early contractures of the elbows, Achilles tendons and spine, slowly progressive muscle wasting and cardiomyopathy associated with cardiac conduction defect. The autosomal dominant form is caused by mutations in the...
Main Author: | Motsch, Isabell |
---|---|
Format: | Doctoral Thesis |
Language: | English |
Published: |
2005
|
Subjects: | |
Online Access: | https://opus.bibliothek.uni-wuerzburg.de/frontdoor/index/index/docId/1315 http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-15360 https://nbn-resolving.org/urn:nbn:de:bvb:20-opus-15360 https://opus.bibliothek.uni-wuerzburg.de/files/1315/Dissertation_Isabell_Motsch.pdf |
Similar Items
-
Dysfunctional lamins as mediators of oxidative stress in Emery-Dreifuss muscular dystrophy
by: Irena Niebroj-Dobosz, et al.
Published: (2017-09-01) -
Emery-Dreifuss muscular dystrophy: the most recognizable laminopathy
by: Agnieszka Madej-Pilarczyk, et al.
Published: (2016-03-01) -
Perinatal Management of Pregnancy Complicated by Autosomal Dominant Emery–Dreifuss Muscular Dystrophy
by: Megumi Sato, et al.
Published: (2016-03-01) -
Emery-Dreifuss muscular dystrophy-associated FHL1 gene mutations : study of molecular and functional consequences in skeletal muscle
by: Ziat, Esma
Published: (2015) -
Defects in the nuclear proteins, emerin and lamins, lead to Emery-Dreifuss muscular dystrophy
by: Fairley, E. A. L.
Published: (2001)