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- W2493852796 abstract "Spinocerebellar ataxia Type 4 (SCA4) is a rare spinocerebellar ataxia characterized not only by cerebellar ataxia but also peripheral neuropathy and pyramidal tract involvement. The clinical manifestations include cerebellar ataxia such as ataxic gait, limb ataxia and dysarthria, loss of deep sensation and areflexia due to axonal sensory neuropathy, and occasional extensor plantar responses. In SCA4, the gene locus is mapped to chromosome 16q22.1. The same locus is demonstrated to show linkage in several Japanese families presenting with autosomal dominant pure cerebellar ataxia or cortical cerebellar atrophy (ADCCA). The 16q-linked ADCCA may be allelic to SCA4." @default.
- W2493852796 created "2016-08-23" @default.
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- W2493852796 date "2003-01-01" @default.
- W2493852796 modified "2023-09-26" @default.
- W2493852796 title "Spinocerebellar Ataxia Type 4 (SCA4)" @default.
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- W2493852796 doi "https://doi.org/10.1016/b978-012566652-7/50008-3" @default.
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