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Journal Abstract Search

162 related items for PubMed ID: 3760830

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  • 23. Mutations in SYNE1 lead to a newly discovered form of autosomal recessive cerebellar ataxia.
    Gros-Louis F, Dupré N, Dion P, Fox MA, Laurent S, Verreault S, Sanes JR, Bouchard JP, Rouleau GA.
    Nat Genet; 2007 Jan; 39(1):80-5. PubMed ID: 17159980
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  • 24. An investigation of pyruvate metabolism in patients with cerebellar and spinocerebellar degeneration.
    Livingstone IR, Mastaglia FL, Pennington RJ.
    J Neurol Sci; 1980 Oct; 48(1):123-32. PubMed ID: 6893466
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  • 25. [Familial Mediterranean fever with pseudodominant inheritance].
    Tarp BD, Obel N.
    Ugeskr Laeger; 2000 Nov 13; 162(46):6261-2. PubMed ID: 11107991
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  • 32. [Medico-genetic study of the population of Uzbekistan. VII. Variability of hereditary pathology in 4 regions of Khorezm province].
    Ginter EK, Budagova KA, Revazov AA, Krasnopol'skaia KD, Dadali EL.
    Genetika; 1986 Feb 13; 22(2):312-21. PubMed ID: 2937687
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  • 37. Electrophysiological studies in familial spastic paraplegia.
    McLeod JG, Morgan JA, Reye C.
    J Neurol Neurosurg Psychiatry; 1977 Jun 13; 40(6):611-5. PubMed ID: 903776
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  • 39. [Optic neuropathy in Strumpell-Lorrain disease: presentation of a clinical case and literature review].
    Makhoul J, Cordonnier M, Van Nechel C.
    Bull Soc Belge Ophtalmol; 2002 Jun 13; (286):9-14. PubMed ID: 12564312
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