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A complex form of hereditary spastic paraplegia harboring a novel variant, p.W1515*, in the SPG11 gene.
Daida, Kensuke; Nishioka, Yosuke; Li, Yuanzhe; Yoshino, Hiroyo; Funayama, Manabu; Hattori, Nobutaka; Nishioka, Kenya.
Affiliation
  • Daida K; Department of Neurology, Juntendo University School of Medicine, 2-1-1 Hongo, Bunkyo-ku, Tokyo 113-8421, Japan.
  • Nishioka Y; Nishioka Memorial Central Clinic, 375 Hasama, Isobecho, Shima-shi, Mie 517-0214, Japan.
  • Li Y; Department of Neurology, Juntendo University School of Medicine, 2-1-1 Hongo, Bunkyo-ku, Tokyo 113-8421, Japan.
  • Yoshino H; Research Institute for Diseases of Old Age, Graduate School of Medicine, Juntendo University, 2-1-1 Hongo, Bunkyo-ku, Tokyo 113-8421, Japan.
  • Funayama M; Department of Neurology, Juntendo University School of Medicine, 2-1-1 Hongo, Bunkyo-ku, Tokyo 113-8421, Japan.
  • Hattori N; Research Institute for Diseases of Old Age, Graduate School of Medicine, Juntendo University, 2-1-1 Hongo, Bunkyo-ku, Tokyo 113-8421, Japan.
  • Nishioka K; Department of Neurology, Juntendo University School of Medicine, 2-1-1 Hongo, Bunkyo-ku, Tokyo 113-8421, Japan.
eNeurologicalSci ; 26: 100391, 2022 Mar.
Article in En | MEDLINE | ID: mdl-35036589
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: ENeurologicalSci Year: 2022 Document type: Article Affiliation country: Japón Country of publication: Países Bajos
Fulltext
Add to My VHL
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: ENeurologicalSci Year: 2022 Document type: Article Affiliation country: Japón Country of publication: Países Bajos