Nodular heterotopia: a rare finding in patients with epilepsy and SCN1A mutation / Heterotopia nodular: um achado raro em pacientes com epilepsia por mutação no gene SCN1A
Arq. neuropsiquiatr
;
79(10): 936-937, Oct. 2021. graf
Article
in English
| LILACS
| ID: biblio-1345314
Full text:
Available
Index:
LILACS (Americas)
Main subject:
Epilepsy
Type of study:
Diagnostic study
Limits:
Humans
Language:
English
Journal:
Arq. neuropsiquiatr
Journal subject:
Neurology
/
Psychiatry
Year:
2021
Type:
Article
Affiliation country:
Brazil
Institution/Affiliation country:
Universidade de Brasília/BR
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