Autosomal Dominant Leukodystrophy: A Disease of the Nuclear Lamina
Author:
Funder
National Institutes of Health
Publisher
Frontiers Media SA
Subject
Cell Biology,Developmental Biology
Reference34 articles.
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2. Oxidative stress induces an ATM-independent senescence pathway through p38 MAPK-mediated lamin B1 accumulation.;Barascu;EMBO J.,2012
3. Messenger RNA processing is altered in autosomal dominant leukodystrophydagger.;Bartoletti-Stella;Hum. Mol. Genet.,2015
4. A family with autosomal dominant leukodystrophy linked to 5q23.2-q23.3 without lamin B1 mutations.;Brussino;Eur. J. Neurol.,2009
5. Genetic localization of an autosomal dominant leukodystrophy mimicking chronic progressive multiple sclerosis to chromosome 5q31.;Coffeen;Hum. Mol. Genet.,2000
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