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Catecholamine Metabolites Affected by the Copper- Dependent Enzyme Dopamine- Beta-Hydroxylase Provide Sensitive Biomarkers for Early Diagnosis of Menkes Disease and Viral-Mediated ATP7A Gene Therapy

Menkes disease is a lethal X-linked recessive disorder of copper metabolism caused by mutations in ATP7A, a copper-transporting ATPase with diverse and important biological functions. Partial deficiency of dopamine-beta-hydroxylase is a biochemical hallmark of this illness due to the normal role of...

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Shranjeno v:
Bibliografske podrobnosti
izdano v:Adv Pharmacol
Main Authors: Kaler, Stephen G., Holmes, Courtney S.
Format: Artigo
Jezik:Inglês
Izdano: 2013
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC6421562/
https://ncbi.nlm.nih.gov/pubmed/24054147
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/B978-0-12-411512-5.00011-7
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