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Aceruloplasminemia: A Severe Neurodegenerative Disorder Deserving an Early Diagnosis
Aceruloplasminemia (ACP) is a rare, adult-onset, autosomal recessive disorder, characterized by systemic iron overload due to mutations in the Ceruloplasmin gene (CP), which in turn lead to absence or strong reduction of CP activity. CP is a ferroxidase that plays a key role in iron export from vari...
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| Publicado en: | Front Neurosci |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Frontiers Media S.A.
2019
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6460567/ https://ncbi.nlm.nih.gov/pubmed/31024241 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fnins.2019.00325 |
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