Afișare rezultate
Afisarea articolelor 1-2(2) pentru cuvîntul-cheie "leukodystrophy" 
| Mutations in NKX6-2 Cause Progressive Spastic Ataxia and Hypomyelination |
| Chelban Viorica12, Patel Nisha3 |
| 2 Emergency Institute of Medicine, |
| American Journal of Human Genetics |
| Nr. 6(100) / 2017 / ISSN 0002-9297 |
| Disponibil online 21 February, 2018. Descarcări-1. Vizualizări-647 |
| Genetic and phenotypic characterization of NKX6-2-related spastic ataxia and hypomyelination |
| Chelban Viorica12, Alsagob M.3, Groppa Stanislav2 |
| 2 Emergency Institute of Medicine, 3 Department of Genetics, KFSHRC, Riyadh |
| European Journal of Neurology |
| Nr. 2(27) / 2020 / ISSN 1351-5101 /ISSNe 1468-1331 |
| Disponibil online 12 March, 2020. Descarcări-0. Vizualizări-956 |
    |
1-2 of 2
