Lhermitte-Duclos disease with concomitant KCNT2 gene mutation: report of an extremely rare combination.
Childs Nerv Syst
; 39(11): 3295-3299, 2023 11.
Article
in En
| MEDLINE
| ID: mdl-37368068
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Hamartoma Syndrome, Multiple
/
Cerebellar Neoplasms
/
Epilepsy
Limits:
Child
/
Humans
/
Male
Language:
En
Journal:
Childs Nerv Syst
Journal subject:
NEUROLOGIA
/
PEDIATRIA
Year:
2023
Document type:
Article
Affiliation country:
Greece
Country of publication:
Germany