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. 2010 Jul;16(6):420-2.
doi: 10.1016/j.parkreldis.2010.03.003. Epub 2010 Apr 22.

Substantia nigra hyperechogenicity in DYT6 dystonia: a pilot study

Substantia nigra hyperechogenicity in DYT6 dystonia: a pilot study

Rachel Saunders-Pullman et al. Parkinsonism Relat Disord. 2010 Jul.
No abstract available

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References

    1. Fuchs T, Gavarini S, Saunders-Pullman R, Raymond D, Ehrlich ME, Bressman SB, et al. Mutations in the THAP1 gene are responsible for DYT6 primary torsion dystonia. Nat Genet. 2009;41:286–8. - PubMed
    1. Bressman SB, Raymond D, Fuchs T, Heiman GA, Ozelius LJ, Saunders-Pullman R. Mutations in THAP1 (DYT6) in early-onset dystonia: a genetic screening study. Lancet Neurol. 2009;8:441–6. - PMC - PubMed
    1. Saunders-Pullman R, Raymond D, Senthil G, Kramer P, Ohmann E, Deligtisch A, et al. Narrowing the DYT6 Region and Evidence for Locus Heterogenity in the Amish-Mennonites. Am J Med Genet A. 2007;143A:2098–105. - PubMed
    1. Hagenah JM, Hedrich K, Becker B, Pramstaller PP, Seidel G, Klein C. Distinguishing early-onset PD from dopa-responsive dystonia with transcranial sonography. Neurology. 2006;66:1951–2. - PubMed
    1. Roussigne M, Cayrol C, Clouaire T, Amalric T, Girard JP. THAP1 is a nuclear proapoptotic factor that links prostate-apoptosis-response-4 (Par-4) to PML nuclear bodies. Oncogene. 2003;22:2432–2442. - PubMed

Publication types

Supplementary concepts