v1
Familial partial epilepsy with variable foci: clinical features and linkage to chromosome 22q12.
Identifier:nobleid.org/w1/20260515/CCBAB784
Type:Journal Article
0 views
Embeddable Badge
[](https://nobleid.org/work/w1/20260515/CCBAB784)
Bibliometric Analysis
Impact metrics, research fronts, co-authorship networks →