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Mutations in SLC30A10 cause parkinsonism and dystonia with hypermanganesemia, polycythemia, and chronic liver disease.
Quadri, Marialuisa; Federico, Antonio; Zhao, Tianna; Breedveld, Guido J; Battisti, Carla; Delnooz, Cathérine; Severijnen, Lies-Anne; Di Toro Mammarella, Lara; Mignarri, Andrea; Monti, Lucia; Sanna, Antioco; Lu, Peng; Punzo, Francesca; Cossu, Giovanni; Willemsen, Rob; Rasi, Fabrizio; Oostra, Ben A; van de Warrenburg, Bart P; Bonifati, Vincenzo.
Affiliation
  • Quadri M; Department of Clinical Genetics, Erasmus MC, Rotterdam, The Netherlands.
Am J Hum Genet ; 90(3): 467-77, 2012 Mar 09.
Article in En | MEDLINE | ID: mdl-22341971
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Full text: 1 Database: MEDLINE Main subject: Membrane Transport Proteins / Parkinsonian Disorders / Manganese Poisoning / Cation Transport Proteins / Metabolic Diseases Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: Am J Hum Genet Year: 2012 Type: Article Affiliation country: Netherlands
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Full text: 1 Database: MEDLINE Main subject: Membrane Transport Proteins / Parkinsonian Disorders / Manganese Poisoning / Cation Transport Proteins / Metabolic Diseases Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: Am J Hum Genet Year: 2012 Type: Article Affiliation country: Netherlands