Á lódáil...
Congenital absence of norepinephrine due to CYB561 mutations
OBJECTIVE: Cytochrome b561 (CYB561) generates ascorbic acid, a cofactor in the enzymatic conversion of dopamine to norepinephrine by dopamine β-hydroxylase. We propose that the clinical relevance of this pathway can be revealed by characterizing the autonomic and biochemical characteristics of patie...
Na minha lista:
| Foilsithe in: | Neurology |
|---|---|
| Main Authors: | , , , , , , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
Lippincott Williams & Wilkins
2020
|
| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6988982/ https://ncbi.nlm.nih.gov/pubmed/31822578 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/WNL.0000000000008734 |
| Clibeanna: |
Cuir Clib Leis
Gan Chlibeanna, Bí ar an gcéad duine leis an taifead seo a chlibeáil!
|