Gain-of-function mutation in ACOX1, Mitchell Syndrome: Gain-of-function mutation in peroxisomal acyl-CoA oxidase 1 (ACOX1) is a very rare heterozygous missense variant (p
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In summary, catalpol demonstrates significant potential as a disposal for brain diseases, including MPTP-induced Parkinsons disease, middle cerebral artery occlusion, subarachnoid hemorrhage, cerebral ischemia induced by electrocoagulation, and neurological damage from thread embolism
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