Heterozygous carriers of galactocerebrosidase mutations that cause Krabbe disease have impaired microglial function and defective repair of myelin damage

Nicole J. Scott-Hewitt; Christopher J. Folts; Mark D. Noble

doi:10.4103/1673-5374.228712

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Home>Articles>Heterozygous carriers of galactocerebrosidase mutations that cause Krabbe disease have impaired microglial function and defective repair of myelin damage

DOI: 10.4103/1673-5374.228712

Heterozygous carriers of galactocerebrosidase mutations that cause Krabbe disease have impaired microglial function and defective repair of myelin damage

Nicole J. Scott-Hewitt

Christopher J. Folts

Mark D. Noble

Keywords：vulnerability locusmultiple sclerosisKrabbe diseasegalactocerebrosidasemicrogliamyelin repairlysosomal storage disordersheterozygous carriersTrem2demyelination

Publication Date：2018-01-01

Online Publishing Date：2025-08-15(First online date of this platform, not the publication date of the document)

Pages：9( 393-401 )

Neural Regeneration Research

ISTICSCI

ISSN：1673-5374

Year, Vol.(Issue)：2018,13(3)