CPT1A plays a key role in the development and treatment of multiple sclerosis and experimental autoimmune encephalomyelitis
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DOI: 10.1038/s41598-019-49868-6
Abstract: Human mutations in carnitine palmitoyl transferase 1A (CPT1A) are correlated with a remarkably low prevalence of multiple sclerosis (MS) in Inuits (P479L) and Hutterites (G710E). To elucidate the role of CPT1A, we established a Cpt1a… read more here.
Keywords: cpt1a p479l; p479l; disease; role ... See more keywords