Hereditary sensory neuropathy type 1-associated deoxysphingolipids cause neurotoxicity, acute calcium handling abnormalities and mitochondrial dysfunction in vitro. (2018)
Attributed to:
HSN1 secondary to SPTLC1/2 mutations: Pathogenesis and treatment
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1016/j.nbd.2018.05.008
PubMed Identifier: 29778900
Publication URI: http://europepmc.org/abstract/MED/29778900
Type: Journal Article/Review
Volume: 117
Parent Publication: Neurobiology of disease
ISSN: 0969-9961