An Altered Sphingolipid Profile as a Risk Factor for Progressive Neurodegeneration in Long-Chain 3-Hydroxyacyl-CoA Deficiency (LCHADD)

Long-chain 3-hydroxyacyl-CoA deficiency (LCHADD) and mitochondrial trifunctional protein (MTPD) belong to a group of inherited metabolic diseases affecting the degradation of long-chain chain fatty acids. During metabolic decompensation the incomplete degradation of fatty acids results in life-threa...

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Detalles Bibliográficos
Autor principal: Tucci, Sara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Hypothesis
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9266703/
https://www.ncbi.nlm.nih.gov/pubmed/35806149
http://dx.doi.org/10.3390/ijms23137144

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9266703/
https://www.ncbi.nlm.nih.gov/pubmed/35806149
http://dx.doi.org/10.3390/ijms23137144

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