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Author/Creator Namekawa, Michito

2. A homozygous mutation of C12orf65 causes spastic paraplegia with optic atrophy and neuropathy (SPG55). Issue 12 (27th November 2012)

Authors:
Shimazaki, Haruo; Takiyama, Yoshihisa; Ishiura, Hiroyuki; Sakai, Chika; Matsushima, Yuichi; Hatakeyama, Hideyuki; Honda, Junko; Sakoe, Kumi; Naoi, Tametou; Namekawa, Michito; Fukuda, Yoko; Takahashi, Yuji; Goto, Jun; Tsuji, Shoji; Goto, Yu-ichi; Nakano, Imaharu
Journal:
Journal of medical genetics
Issue:
Volume 49:Issue 12(2012)
Page Start:
777
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. Autosomal-recessive complicated spastic paraplegia with a novel lysosomal trafficking regulator gene mutation. Issue 9 (12th February 2014)

Authors:
Shimazaki, Haruo; Honda, Junko; Naoi, Tametou; Namekawa, Michito; Nakano, Imaharu; Yazaki, Masahide; Nakamura, Katsuya; Yoshida, Kunihiro; Ikeda, Shu-ichi; Ishiura, Hiroyuki; Fukuda, Yoko; Takahashi, Yuji; Goto, Jun; Tsuji, Shoji; Takiyama, Yoshihisa
Journal:
Journal of neurology, neurosurgery and psychiatry
Issue:
Volume 85:Issue 9(2014)
Page Start:
1024
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗