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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...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Front Neurosci |
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| Κύριοι συγγραφείς: | , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Frontiers Media S.A.
2019
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| Θέματα: | |
| Διαθέσιμο Online: | 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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