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Author/Creator Kita, Yasushi

1. A homozygous mutation of VWA3B causes cerebellar ataxia with intellectual disability. Issue 6 (8th July 2015)

Authors:
Kawarai, Toshitaka; Tajima, Atsushi; Kuroda, Yukiko; Saji, Naoki; Orlacchio, Antonio; Terasawa, Hideo; Shimizu, Hirotaka; Kita, Yasushi; Izumi, Yuishin; Mitsui, Takao; Imoto, Issei; Kaji, Ryuji
Journal:
Journal of neurology, neurosurgery and psychiatry
Issue:
Volume 87:Issue 6(2016)
Page Start:
656
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

4. Spinocerebellar ataxia type 36 exists in diverse populations and can be caused by a short hexanucleotide GGCCTG repeat expansion. Issue 9 (4th December 2014)

Authors:
Obayashi, Masato; Stevanin, Giovanni; Synofzik, Matthis; Monin, Marie-Lorraine; Duyckaerts, Charles; Sato, Nozomu; Streichenberger, Nathalie; Vighetto, Alain; Desestret, Virginie; Tesson, Christelle; Wichmann, H-Erich; Illig, Thomas; Huttenlocher, Johanna; Kita, Yasushi; Izumi, Yuishin; Mizusawa,...
Journal:
Journal of neurology, neurosurgery and psychiatry
Issue:
Volume 86:Issue 9(2015)
Page Start:
986
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗