Spinocerebellar ataxia 8: variable phenotype and unique pathogenesis.
about
Bolivian kindred with combined spinocerebellar ataxia types 2 and 10.Hereditary ataxias: overview.RNA toxicity and foci formation in microsatellite expansion diseases.Non-Ataxic Phenotypes of SCA8 Mimicking Amyotrophic Lateral Sclerosis and Parkinson Disease.Genetic screening of Greek patients with Huntington’s disease phenocopies identifies an SCA8 expansion.Altered GABAergic system in the living brain of a patient with spinocerebellar ataxia type 8.
P2860
Spinocerebellar ataxia 8: variable phenotype and unique pathogenesis.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
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scientific article published on 25 June 2009
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vedecký článok
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vetenskaplig artikel
@sv
videnskabelig artikel
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vědecký článek
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name
Spinocerebellar ataxia 8: variable phenotype and unique pathogenesis.
@en
Spinocerebellar ataxia 8: variable phenotype and unique pathogenesis.
@nl
type
label
Spinocerebellar ataxia 8: variable phenotype and unique pathogenesis.
@en
Spinocerebellar ataxia 8: variable phenotype and unique pathogenesis.
@nl
prefLabel
Spinocerebellar ataxia 8: variable phenotype and unique pathogenesis.
@en
Spinocerebellar ataxia 8: variable phenotype and unique pathogenesis.
@nl
P1476
Spinocerebellar ataxia 8: variable phenotype and unique pathogenesis.
@en
P2093
Amitabh Gupta
P304
P356
10.1016/J.PARKRELDIS.2009.06.001
P577
2009-06-25T00:00:00Z