Pathology of inherited manganese transporter deficiency-Reference-Cited by-同舟云学术

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Pathology of inherited manganese transporter deficiency

Published:2014-04 Issue:4 Volume:75 Page:608-612
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Lechpammer Mirna¹,Clegg Michael S.²,Muzar Zukhrofi¹,Huebner Philip A.¹,Jin Lee-Way¹,Gospe Sidney M.³

Affiliation:

1. Department Pathology and Laboratory Medicine; University of California, Davis Medical Center; Sacramento CA

2. Department of Food Science and Technology; University of California; Davis CA

3. Departments of Neurology and Pediatrics; University of Washington and Seattle Children's Hospital; Seattle WA

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference19 articles.

1. Paraparesis, hypermanganesaemia, and polycythaemia: a novel presentation of cirrhosis;Gospe;Arch Dis Child,2000

2. Mutations in SLC30A10 cause parkinsonism and dystonia with hypermanganesemia, polycythemia, and chronic liver disease;Quadri;Am J Hum Genet,2012

3. Syndrome of hepatic cirrhosis, dystonia, polycythemia, and hypermanganesemia caused by mutations in SLC30A10, a manganese transporter in man;Tuschl;Am J Hum Genet,2012

4. Dystonia with brain manganese accumulation resulting from SLC30A10 mutations: a new treatable disorder;Stamelou;Mov Disord,2012

5. Hepatic cirrhosis, dystonia, polycythaemia and hypermanganesaemia-a new metabolic disorder;Tuschl;J Inherit Metab Dis,2008

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