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- Title
Familial Hypermanganesemia in Iran.
- Authors
Tabatabaee, Seyedeh Narges; Effat Nejad, Sajjad; Nikkhah, Ali; Hashemi, Narges; Alavi, Afagh; Lang, Anthony E.; Rohani, Mohammad; Emamikhah, Maziar
- Abstract
Keywords: familial hypermanganesemia; SLC30A10 gene; SLC39A14 gene; manganese; dystonia EN familial hypermanganesemia SLC30A10 gene SLC39A14 gene manganese dystonia 850 853 4 05/18/23 20230501 NES 230501 We read with interest the recent report of Garg et al[1] on familial hypermanganesemia. SLC30A10 gene, familial hypermanganesemia, manganese, dystonia, SLC39A14 gene Mutations in SLC39A14 disrupt manganese homeostasis and cause childhood-onset parkinsonism-dystonia.
- Subjects
IRAN; MOVEMENT disorders; DENTATE nucleus; GLOBUS pallidus
- Publication
Movement Disorders Clinical Practice, 2023, Vol 10, Issue 5, p850
- ISSN
2330-1619
- Publication type
Article
- DOI
10.1002/mdc3.13723