Congenital Neuronal Ceroid Lipofuscinosis with a Novel CTSD Gene Mutation: A Rare Cause of Neonatal-Onset Neurodegenerative Disorder.
Neuropediatrics
; 49(2): 150-153, 2018 04.
Article
in En
| MEDLINE
| ID: mdl-29284168
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Cathepsin D
/
Mutation
/
Neuronal Ceroid-Lipofuscinoses
Limits:
Female
/
Humans
/
Infant
Language:
En
Journal:
Neuropediatrics
Year:
2018
Document type:
Article