scholarly article | Q13442814 |
P356 | DOI | 10.1007/S00415-009-0015-2 |
P698 | PubMed publication ID | 19259763 |
P50 | author | Huw R Morris | Q42586947 |
Mark Wardle | Q60680030 | ||
Mustapha Muzaimi | Q61201541 | ||
P2093 | author name string | Neil P Robertson | |
Nigel M Williams | |||
Elisa Majounie | |||
P2860 | cites work | ??? | Q64789962 |
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Frequency analysis of autosomal dominant cerebellar ataxias in Japanese patients and clinical characterization of spinocerebellar ataxia type 6 | Q28268233 | ||
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The role of the SCA2 trinucleotide repeat expansion in 89 autosomal dominant cerebellar ataxia families. Frequency, clinical and genetic correlates | Q48486744 | ||
FMR1 gene premutation is a frequent genetic cause of late-onset sporadic cerebellar ataxia. | Q50282467 | ||
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Are (CTG)n expansions at the SCA8 locus rare polymorphisms? | Q57970937 | ||
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Genetic background of apparently idiopathic sporadic cerebellar ataxia | Q73074693 | ||
Molecular analysis of autosomal dominant hereditary ataxias in the Indian population: high frequency of SCA2 and evidence for a common founder mutation | Q73621643 | ||
Difference in disease-free survival curve and regional distribution according to subtype of spinocerebellar ataxia: a study of 1,286 Japanese patients | Q74457553 | ||
The occurrence of dominant spinocerebellar ataxias among 251 Finnish ataxia patients and the role of predisposing large normal alleles in a genetically isolated population | Q81361572 | ||
P433 | issue | 3 | |
P304 | page(s) | 343-348 | |
P577 | publication date | 2009-03-06 | |
P1433 | published in | Journal of Neurology | Q6295649 |
P1476 | title | The genetic aetiology of late-onset chronic progressive cerebellar ataxia. A population-based study | |
P478 | volume | 256 |
Q42591553 | Contactin-associated protein-2 antibodies in non-paraneoplastic cerebellar ataxia |
Q35061105 | FXTAS is rare among Portuguese patients with movement disorders: FMR1 premutations may be associated with a wider spectrum of phenotypes |
Q38896237 | Fragile X-associated tremor/ataxia syndrome: phenotypic comparisons with other movement disorders |
Q34329664 | Fragile x-associated tremor ataxia syndrome: the expanding clinical picture, pathophysiology, epidemiology, and update on treatment |
Q54396826 | Late onset Alexander's disease presenting as cerebellar ataxia associated with a novel mutation in the GFAP gene. |
Q44848424 | Leukodystrophies in idiopathic adult-onset ataxia: frequency and phenotype in 105 patients |
Q38194974 | Multiple system atrophy of the cerebellar type: clinical state of the art. |
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Q45073197 | Quantitative trait loci mapping for conjugated linoleic acid, vaccenic acid and ∆(9) -desaturase in Italian Brown Swiss dairy cattle using selective DNA pooling |
Q44457611 | The Diagnosis and Natural History of Multiple System Atrophy, Cerebellar Type |
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