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Results 1 - 10 of 26 for Dystonia 10
  1. TOR1A gene 
    ... P. Developments in the molecular biology of DYT1 dystonia. Mov Disord. 2003 Oct;18(10):1102-7. doi: 10.1002/mds.10549. Citation ...
    https://medlineplus.gov/genetics/gene/tor1a - Genetics
  2. THAP1 gene 
    ... DYT6) are an additional cause of early-onset dystonia. Neurology. 2010 Mar 9;74(10):846-50. doi: 10.1212/WNL.0b013e3181d5276d. Citation ... R, Hadjigeorgiou GM, Bhatia KP. THAP1 mutations and dystonia phenotypes: genotype ... Mov Disord. 2012 Sep 1;27(10):1290-4. doi: 10.1002/mds.25146. Epub ...
    https://medlineplus.gov/genetics/gene/thap1 - Genetics
  3. GCH1 gene 
    ... guanosine triphosphate cyclohydrolase 1 gene associated with DYT5 dystonia. Arch Neurol. 2006 Nov;63(11):1605-10. doi: 10.1001/archneur.63.11.1605. Citation ...
    https://medlineplus.gov/genetics/gene/gch1 - Genetics
  4. PRKRA gene 
    ... exome sequencing identifies PRKRA mutations in a European dystonia family. Mov Disord. 2014 Oct;29(12):1504-10. doi: 10.1002/mds.25981. Epub 2014 Aug ...
    https://medlineplus.gov/genetics/gene/prkra - Genetics
  5. PLA2G6 gene 
    ... Central Schneider SA, Bhatia KP. Rare causes of dystonia parkinsonism. Curr Neurol Neurosci Rep. 2010 Nov;10(6):431-9. doi: 10.1007/s11910-010- ...
    https://medlineplus.gov/genetics/gene/pla2g6 - Genetics
  6. ATP1A3 gene 
    ... alpha3 gene ATP1A3 are associated with rapid-onset dystonia parkinsonism. Neuron. 2004 Jul 22;43(2):169-75. doi: 10.1016/j.neuron.2004.06.028. Citation on ...
    https://medlineplus.gov/genetics/gene/atp1a3 - Genetics
  7. TH gene 
    ... hydroxylase deficiency causes progressive encephalopathy and dopa-nonresponsive dystonia. Ann Neurol. 2003;54 Suppl 6:S56-65. doi: 10.1002/ana.10632. Citation on PubMed Pearl PL, ...
    https://medlineplus.gov/genetics/gene/th - Genetics
  8. SPR gene 
    ... gene (SPR) in a patient with dopa-responsive dystonia. Neurogenetics. 2004 Sep;5(3):187-90. doi: 10.1007/s10048-004-0182-3. Epub 2004 Jul ...
    https://medlineplus.gov/genetics/gene/spr - Genetics
  9. SERAC1 gene 
    ... mitochondrial function and intracellular cholesterol trafficking and cause dystonia and deafness. Nat Genet. 2012 Jun 10;44(7):797-802. doi: 10.1038/ng. ...
    https://medlineplus.gov/genetics/gene/serac1 - Genetics
  10. TIMM8A gene 
    ... patient with a novel mutation in the deafness-dystonia peptide (DDP1) gene. Brain. 2003 Aug;126(Pt 8):1814-20. doi: 10.1093/brain/awg174. Epub 2003 Jun 4. Citation ...
    https://medlineplus.gov/genetics/gene/timm8a - Genetics
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