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Article
Open AccessA case report of SPG11 mutations in a Chinese ARHSP-TCC family
Autosomal recessive hereditary spastic paraplegia (ARHSP) with thin corpus callosum (TCC) is a complicated form of hereditary spastic paraplegia, characterized by progressive spastic paraplegia, weakness of th...
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Correction to: SPG7 and Impaired Emotional Communication
The original version of this article unfortunately contained an incorrect assignment of affiliations of Linwei Zhang and Tetsuo Ashizawa.