Hereditary sensory neuropathy type 1-associated deoxysphingolipids cause neurotoxicity, acute calcium handling abnormalities and mitochondrial dysfunction in vitro. (2018)

First Author: Wilson ER
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