Haruo Shimazaki
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4CO-AUTHORS
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Publications (4)
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|Dec 27, 2019
VPS13D-related disorders presenting as a pure and complicated form of hereditary spastic paraplegia.Kishin Koh, Hiroyuki Ishiura, Haruo Shimazaki
|Jun 20, 2018
Novel mutations in the ALDH18A1 gene in complicated hereditary spastic paraplegia with cerebellar ataxia and cognitive impairment.Kishin Koh, Hiroyuki Ishiura, Minako Beppu
|Feb 14, 2014
Autosomal-recessive complicated spastic paraplegia with a novel lysosomal trafficking regulator gene mutation.Haruo Shimazaki, Junko Honda, Tametou Naoi
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