A Novel Mutation Related to Aceruloplasminemia with Mild Clinical Findings: A Case Report
<b>Background and Clinical Significance</b>: Aceruloplasminemia (ACP), a member of the neurodegeneration with brain iron accumulation (NBIA) spectrum of disorders, is a rare disorder caused by mutations in the ceruloplasmin (CP) gene. Iron accumulation in various organs, including the br...
Saved in:
| Main Authors: | , , , , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
MDPI AG
2024-12-01
|
| Series: | Reports |
| Subjects: | |
| Online Access: | https://www.mdpi.com/2571-841X/8/1/4 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|