Molecular genetic investigations identify new clinical phenotypes associated with BCS1L-related mitochondrial disease.
Hum Mol Genet
; 28(22): 3766-3776, 2019 11 15.
Article
in En
| MEDLINE
| ID: mdl-31435670
Full text:
1
Database:
MEDLINE
Main subject:
Electron Transport Complex III
/
Mitochondrial Diseases
/
ATPases Associated with Diverse Cellular Activities
Type of study:
Prognostic_studies
/
Risk_factors_studies
Limits:
Adult
/
Female
/
Humans
/
Infant
/
Male
Language:
En
Journal:
Hum Mol Genet
Journal subject:
BIOLOGIA MOLECULAR
/
GENETICA MEDICA
Year:
2019
Type:
Article
Affiliation country:
United kingdom