Afișare rezultate
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-639 |
Genotype-phenotype correlations, dystonia and disease progression in spinocerebellar ataxia type 14 |
Chelban Viorica123, Wiethoff Sarah14 |
3 Emergency Institute of Medicine, |
Movement Disorders |
Nr. 7(33) / 2018 / ISSN 0885-3185 /ISSNe 1531-8257 |
Disponibil online 8 December, 2018. Descarcări-0. Vizualizări-675 |
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