A SLC39A8 variant causes manganese deficiency, and glycosylation and mitochondrial disorders.
J Inherit Metab Dis
; 40(2): 261-269, 2017 03.
Article
in En
| MEDLINE
| ID: mdl-27995398
Full text:
1
Database:
MEDLINE
Main subject:
Genetic Variation
/
Mitochondrial Diseases
/
Cation Transport Proteins
/
Manganese
Type of study:
Etiology_studies
/
Prognostic_studies
Limits:
Child
/
Female
/
Humans
/
Infant
Language:
En
Journal:
J Inherit Metab Dis
Year:
2017
Type:
Article
Affiliation country:
Australia