Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

SLC39A14 mutations expand the spectrum of manganese transporter defects causing parkinsonism-dystonia.

Movement disorders : official journal of the Movement Disorder Society - 1 Nov 2016

Balint Bettina, Bhatia Kailash P

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Dystonia
Share to Dystonic Disorders
Share to Manganese
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Parkinsonian Disorders

Source

Identifiers

PMID: 27739105
DOI: 10.1002/mds.26821

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

SLC39A14 mutations expand the spectrum of manganese transporter defects causing parkinsonism-dystonia.PMID 27739105Read ↗

Novel founder intronic variant in SLC39A14 in two families causing Manganism and potential treatment strategies.Semantic proximity Read ↗

Hereditary Disorders of Manganese Metabolism: Pathophysiology of Childhood-Onset Dystonia-Parkinsonism in SLC39A14 Mutation Carriers and Genetic Animal Models.Semantic proximity Read ↗

Mutations in SLC39A14 disrupt manganese homeostasis and cause childhood-onset parkinsonism-dystonia.Semantic proximity Read ↗

Hypermanganesemia due to mutations in SLC39A14: further insights into Mn deposition in the central nervous system.Semantic proximity Read ↗

Manganese Neurotoxicity: A Comprehensive Review of Pathophysiology and Inherited and Acquired DisordersSemantic proximity Read ↗

Familial manganese-induced neurotoxicity due to mutations in SLC30A10 or SLC39A14.Semantic proximity Read ↗

Primary and secondary dystonic syndromes: an update.Semantic proximity Read ↗

A humanized neuronal model system reveals key roles for manganese in neuronal endocytosis, calcium flux and mitochondrial bioenergeticsSemantic proximity Read ↗

Effect of Chelation Therapy on a Korean Patient With Brain Manganese Deposition Resulting From a Compound Heterozygous Mutation in the SLC39A14 GeneSemantic proximity Read ↗

The Functions of ZIP8, ZIP14, and ZnT10 in the Regulation of Systemic Manganese Homeostasis.Semantic proximity Read ↗

Mutations in SLC30A10 cause parkinsonism and dystonia with hypermanganesemia, polycythemia, and chronic liver disease.Semantic proximity Read ↗

Gene symbol: SLC7A9. Disease: cystinuria, type non-I.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.