A case of late-onset riboflavin responsive multiple acyl-CoA dehydrogenase deficiency with novel mutations in ETFDH gene.
CNS Neurosci Ther
; 18(11): 952-4, 2012 Nov.
Article
in En
| MEDLINE
| ID: mdl-23106979
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Electron-Transferring Flavoproteins
/
Multiple Acyl Coenzyme A Dehydrogenase Deficiency
/
Oxidoreductases Acting on CH-NH Group Donors
/
Iron-Sulfur Proteins
/
Mutation
Limits:
Humans
/
Male
/
Middle aged
Language:
En
Journal:
CNS Neurosci Ther
Journal subject:
NEUROLOGIA
/
TERAPEUTICA
Year:
2012
Document type:
Article
Country of publication:
Reino Unido