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Understanding the Ultra-Rare Disease Autosomal Dominant Leukodystrophy: an Updated Review on Morpho-Functional Alterations Found in Experimental Models.
- Published in:
- Molecular Neurobiology, 2023, v. 60, n. 11, p. 6362, doi. 10.1007/s12035-023-03461-1
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- Article
LMNB1 Duplication-Mediated Autosomal Dominant Adult-Onset Leukodystrophy in an Indian Family.
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- Annals of Indian Academy of Neurology, 2021, v. 24, n. 3, p. 413, doi. 10.4103/aian.AIAN_1262_20
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- Article
Deletion of conserved non‐coding sequences downstream from NKX2‐1: A novel disease‐causing mechanism for benign hereditary chorea.
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- Molecular Genetics & Genomic Medicine, 2021, v. 9, n. 4, p. 1, doi. 10.1002/mgg3.1647
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- Article
Defects of Lipid Synthesis Are Linked to the Age-Dependent Demyelination Caused by Lamin B1 Overexpression.
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- Journal of Neuroscience, 2015, v. 35, n. 34, p. 12002, doi. 10.1523/JNEUROSCI.1668-15.2015
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- Article
Lamin B1 mediates cell-autonomous neuropathology in a leukodystrophy mouse model.
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- Journal of Clinical Investigation, 2013, v. 123, n. 7, p. 2719, doi. 10.1172/JCI66737
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- Article
Lamin B1 mediates cell-autonomous neuropathology in a leukodystrophy mouse model.
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- Journal of Clinical Investigation, 2013, v. 123, n. 6, p. 2719, doi. 10.1172/JCI66737
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- Article
Corrigendum: Lamin B1 duplications cause autosomal dominant leukodystrophy.
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- 2007
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- Correction notice
Lamin B1 duplications cause autosomal dominant leukodystrophy.
- Published in:
- Nature Genetics, 2006, v. 38, n. 10, p. 1114, doi. 10.1038/ng1872
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- Article
Functional consequences of a CKIdmutation causing familial advanced sleep phase syndrome.
- Published in:
- Nature, 2005, v. 434, n. 7033, p. 640, doi. 10.1038/nature03453
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- Publication type:
- Article