Galactosylceramidase deficiency and pathological abnormalities in cerebral white matter of Krabbe disease

Author:

Iacono Diego,Koga ShunsukeORCID,Peng Hui,Manavalan Arulmani,Daiker Jessica,Castanedes-Casey Monica,Martin Nicholas B.ORCID,Herdt Aimee R.,Gelb Michael H.,Dickson Dennis W.ORCID,Lee Chris W.ORCID

Publisher

Elsevier BV

Subject

Neurology

Reference51 articles.

1. Fingolimod rescues demyelination in a mouse model of Krabbe’s disease;Bechet;J. Neurosci.,2020

2. Abnormal LAMP1 glycosylation may play a role in Niemann-Pick disease, type C pathology;Cawley;PLoS One,2020

3. Molecular heterogeneity of late-onset forms of globoid-cell leukodystrophy;De Gasperi;Am. J. Hum. Genet.,1996

4. Insights into Krabbe disease from structures of galactocerebrosidase;Deane;Proc. Natl. Acad. Sci. U. S. A.,2011

5. Krabbe disease in adults: phenotypic and genotypic update from a series of 11 cases and a review;Debs;J. Inherit. Metab. Dis.,2013

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