Hypermanganesemia due to mutations in SLC39A14: further insights into Mn deposition in the central nervous system

被引：0
|
作者：
L. Marti-Sanchez
J. D. Ortigoza-Escobar
A. Darling
M. Villaronga
H. Baide
M. Molero-Luis
M. Batllori
M. I. Vanegas
J. Muchart
L. Aquino
R. Artuch
A. Macaya
M. A. Kurian
Pérez Dueñas
机构：
[1] University of Barcelona,Department of Biochemistry, Institut de Recerca
[2] University of Barcelona, Hospital Sant Joan de Déu
[3] University of Barcelona,Department of Child Neurology, Institut de Recerca
[4] University of Barcelona, Hospital Sant Joan de Déu
[5] Deparment of Pediatrics,Department of Pharmacy, Institut de Recerca
[6] Hospital de Mataró, Hospital Sant Joan de Déu
[7] Pediatric Neurology Research Group,Department of Radiology, Institut de Recerca
[8] Vall d’Hebron Research Institute (VHIR), Hospital Sant Joan de Déu
[9] Universitat Autònoma de Barcelona,undefined
[10] Molecular Neurosciences,undefined
[11] Developmental Neurosciences Programme,undefined
[12] UCL-Great Ormond Street Institute of Child Health,undefined
来源：
Orphanet Journal of Rare Diseases | / 13卷
关键词：
Manganese homeostasis; ; ; Dystonia; Pallidum; Hypermanganesemia;
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