Early progression of Krabbe disease in patients with symptom onset between 0 and 5 months

BACKGROUND: Krabbe disease is a rare neurological disorder caused by a deficiency in the lysosomal enzyme, β-galactocerebrosidase, resulting in demyelination of the central and peripheral nervous systems. If left without treatment, Krabbe disease results in progressive neurodegeneration with reduced...

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Detalles Bibliográficos
Autores principales: Beltran-Quintero, Maria L., Bascou, Nicholas A., Poe, Michele D., Wenger, David A., Saavedra-Matiz, Carlos A., Nichols, Matthew J., Escolar, Maria L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6378723/
https://www.ncbi.nlm.nih.gov/pubmed/30777126
http://dx.doi.org/10.1186/s13023-019-1018-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6378723/
https://www.ncbi.nlm.nih.gov/pubmed/30777126
http://dx.doi.org/10.1186/s13023-019-1018-4

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