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Updated: Mar 22, 2026

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A Simple Composite Phenotype Scoring System for Evaluating Mouse Models of Cerebellar Ataxia
Published on: May 21, 2010
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Predominant cerebellar phenotype in spastic paraplegia 7 (SPG7)
Hiroyuki Yahikozawa1, Kunihiro Yoshida2, Shunichi Sato1
1Department of Neurology, Nagano Red Cross Hospital , Nagano, Japan.
Human Genome Variation
|April 16, 2016
Abstract:
We report a Japanese family with spastic paraplegia 7 (SPG7) that carries a deleterious homozygous p.R398X mutation in SPG7. The patients showed a predominant cerebellar ataxia phenotype. SPG7 is quite rare in Japan, but it should be included in the differential diagnosis for hereditary spastic-ataxic syndromes, even if the cerebellar signs are much more pronounced than the pyramidal tract signs.
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