Associated Papers
A novel homozygous SLC39A14 variant in an infant with hypermanganesemia and a review of the literature.
Zhang M et al.
Frontiers in Pediatrics, 2022
Autosomal-recessive iron deficiency anemia, dystonia and hypermanganesemia caused by new variant mutation of the manganese transporter gene SLC39A14.
Zeglam A et al.
Acta Neurologica Belgica, 2019
Genetic Disorders of Manganese Metabolism.
Anagianni S et al.
Current Neurology and Neuroscience Reports, 2019
Mutations in SLC39A14 disrupt manganese homeostasis and cause childhood-onset parkinsonism-dystonia.
Tuschl K et al.
Nature Communications, 2016
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