Associated Papers
Consensus of Expert Opinion for the Diagnosis and Management of Hypermanganesaemia With Dystonia 1 and 2.
Fang S et al.
Journal of Inherited Metabolic Disease, 2025
40320765 (PubMed )
Supplement: JIMD-48-0-s001.xlsx › Sheet1
Case Report: Childhood Erythrocytosis due to Hypermanganesemia Caused by Homozygous SLC30A10 Mutation.
Coppola T et al.
Frontiers in Hematology, 2024
Atypical presentation of SLC30A10 gene mutation with hypermanganesemia, seizures and polycythemia.
Jagadish S et al.
Epilepsy & Behavior Reports, 2021
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