Identification of novel non-HFE mutations in Chinese patients with hereditary hemochromatosis.
Orphanet J Rare Dis
; 17(1): 216, 2022 06 06.
Article
in En
| MEDLINE
| ID: mdl-35668470
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Iron Overload
/
Hemochromatosis
Type of study:
Diagnostic_studies
Limits:
Humans
Country/Region as subject:
Asia
Language:
En
Journal:
Orphanet J Rare Dis
Journal subject:
MEDICINA
Year:
2022
Document type:
Article
Affiliation country:
China
Country of publication:
United kingdom