SLC39A8 and Dystonia: In Patient-1, the analysis of a gene panel associated with dystonia revealed two novel compound heterozygous variants in the SLC39A8 gene (ZIP8, OMIM #608732), c.1048G > A (p. Gly350Arg) and c.131C > G (p.Ser44Trp), inherited from the mother and the father, respectively.