Novel mutations in malonyl-CoA-acyl carrier protein transacylase provoke autosomal recessive optic neuropathy.
Hum Mol Genet
; 29(3): 444-458, 2020 02 01.
Article
in En
| MEDLINE
| ID: mdl-31915829
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Optic Nerve
/
Retinal Ganglion Cells
/
Optic Nerve Diseases
/
Acyl-Carrier Protein S-Malonyltransferase
/
Genes, Recessive
/
Mitochondria
Type of study:
Etiology_studies
Limits:
Animals
/
Child
/
Female
/
Humans
/
Male
Language:
En
Journal:
Hum Mol Genet
Journal subject:
BIOLOGIA MOLECULAR
/
GENETICA MEDICA
Year:
2020
Document type:
Article
Affiliation country:
Country of publication: