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Browsing byAuthor : jaeranlee
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Publication Date2017-10
Autosomal dominant transmission of complicated hereditary spastic paraplegia due to a dominant negative mutation of KIF1A, SPG30 gene.
SCIENTIFIC REPORTS, v.7, no.1, pp.12527 - 12527
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Publication Date2015-01
De novo mutations in the motor domain of KIF1A cause cognitive impairment, spastic paraparesis, axonal neuropathy, and cerebellar atrophy
HUMAN MUTATION, v.36, no.1, pp.69 - 78
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