Investigation on a MMACHC mutant from cblC disease: The c.394C>T variant.
Biochim Biophys Acta Proteins Proteom
; 1870(6): 140793, 2022 06 01.
Article
in En
| MEDLINE
| ID: mdl-35618206
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Amino Acid Metabolism, Inborn Errors
/
Homocystinuria
Type of study:
Diagnostic_studies
Limits:
Child
/
Humans
Language:
En
Journal:
Biochim Biophys Acta Proteins Proteom
Year:
2022
Document type:
Article
Affiliation country:
Italy
Country of publication:
Netherlands