Browsing by Subject Severe phenotype
Showing results 1 to 1 of 1
| Issue Date | Title | Author(s) | Rank |
|---|---|---|---|
| 15-Feb-2013 | Lafora disease: Severe phenotype associated with homozygous deletion of the NHLRC1 gene | Kecmanović, Miljana ; Jović, Nebojša; Čukić, Mirjana; Keckarević Marković, Milica ; Keckarević, Dušan ; Stevanović, Galina; Romac, Stanka |