Biallelic Mutations in TMEM126B Cause Severe Complex I Deficiency with a Variable Clinical Phenotype.
Am J Hum Genet
; 99(1): 217-27, 2016 Jul 07.
Article
in En
| MEDLINE
| ID: mdl-27374774
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Phenotype
/
Mitochondrial Diseases
/
Electron Transport Complex I
/
Alleles
/
Membrane Proteins
/
Mutation
Type of study:
Prognostic_studies
Limits:
Adolescent
/
Adult
/
Child
/
Female
/
Humans
/
Infant
/
Male
/
Middle aged
Language:
En
Journal:
Am J Hum Genet
Year:
2016
Document type:
Article
Affiliation country:
Country of publication: