Cargando…
Structure and Function of the ABCD1 Variant Database: 20 Years, 940 Pathogenic Variants, and 3400 Cases of Adrenoleukodystrophy
The progressive neurometabolic disorder X-linked adrenoleukodystrophy (ALD) is caused by pathogenic variants in the ABCD1 gene, which encodes the peroxisomal ATP-binding transporter for very-long-chain fatty acids. The clinical spectrum of ALD includes adrenal insufficiency, myelopathy, and/or leuko...
Autores principales: | Mallack, Eric J., Gao, Kerry, Engelen, Marc, Kemp, Stephan |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8773697/ https://www.ncbi.nlm.nih.gov/pubmed/35053399 http://dx.doi.org/10.3390/cells11020283 |
Ejemplares similares
-
Evolution of adrenoleukodystrophy model systems
por: Montoro, Roberto, et al.
Publicado: (2021) -
X-Linked Adrenoleukodystrophy: Molecular and Functional Analysis of the ABCD1 Gene in Argentinean Patients
por: Amorosi, Cyntia Anabel, et al.
Publicado: (2012) -
Molecular Biomarkers for Adrenoleukodystrophy: An Unmet Need
por: Honey, Madison I. J., et al.
Publicado: (2021) -
X-linked Adrenoleukodystrophy in a 20-Year-Old Male With an ABCD1 Gene Mutation: First Case From Pakistan
por: Ghori, Mariam, et al.
Publicado: (2022) -
Bezafibrate for X-Linked Adrenoleukodystrophy
por: Engelen, Marc, et al.
Publicado: (2012)