An autopsied case report of spastic paraplegia with thin corpus callosum carrying a novel mutation in the SPG11 gene: widespread degeneration with eosinophilic inclusions

被引：0
作者：
Mika Hayakawa
Tomoyasu Matsubara
Yoko Mochizuki
Chisen Takeuchi
Motoyuki Minamitani
Masayuki Imai
Kenjiro Kosaki
Tomio Arai
Shigeo Murayama
机构：
[1] Tokyo Metropolitan Kita Medical and Rehabilitation Center for the Disabled,Department of Pediatrics
[2] Tokyo Metropolitan Geriatric Hospital and Institute of Gerontology,Department of Neurology and Neuropathology (the Brain Bank for Aging Research)
[3] Tokyo Metropolitan Kita Medical and Rehabilitation Center for the Disabled,Department of Neurology
[4] Keio University School of Medicine,Center for Medical Genetics
[5] Tokyo Metropolitan Geriatric Hospital and Institute of Gerontology,Department of Pathology
[6] Osaka University,The Brain Bank for Neurodevelopmental, Neurological and Psychiatric Disorders, United Graduate School of Child Development
来源：
BMC Neurology | / 22卷
关键词：
Alpha-synuclein; Case report; Hereditary spastic paraplegia with a thin corpus callosum; Lateral geniculate body; Lewy body-related α-synucleinopathy; p62-immunoreactive neuronal cytoplasmic inclusions; gene;
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