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Date 2017 Author/Creator Hashiguchi, A.

1. Clinical and mutational spectrum of Charcot–Marie–Tooth disease type 2Z caused by MORC2 variants in Japan. (3rd August 2017)

Authors:
Ando, M.; Okamoto, Y.; Yoshimura, A.; Yuan, J.‐H.; Hiramatsu, Y.; Higuchi, Y.; Hashiguchi, A.; Mitsui, J.; Ishiura, H.; Fukumura, S.; Matsushima, M.; Ochi, N.; Tsugawa, J.; Morishita, S.; Tsuji, S.; Takashima, H.
Journal:
European journal of neurology
Issue:
Volume 24:Number 10(2017:Oct.)
Page Start:
1274
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

2. Clinical and mutational spectrum of Japanese patients with Charcot‐Marie‐Tooth disease caused by GDAP1 variants. Issue 3 (19th April 2017)

Authors:
Yoshimura, A.; Yuan, J.‐H.; Hashiguchi, A.; Hiramatsu, Y.; Ando, M.; Higuchi, Y.; Nakamura, T.; Okamoto, Y.; Matsumura, K.; Hamano, T.; Sawaura, N.; Shimatani, Y.; Kumada, S.; Okumura, Y.; Miyahara, J.; Yamaguchi, Y.; Kitamura, S.; Haginoya, K.; Mitsui, J.; Ishiura, H.
Journal:
Clinical genetics
Issue:
Volume 92:Issue 3(2017)
Page Start:
274
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. WNK1/HSN2 founder mutation in patients with hereditary sensory and autonomic neuropathy: A Japanese cohort study. Issue 6 (20th July 2017)

Authors:
Yuan, J.‐H.; Hashiguchi, A.; Yoshimura, A.; Sakai, N.; Takahashi, M.P.; Ueda, T.; Taniguchi, A.; Okamoto, S.; Kanazawa, N.; Yamamoto, Y.; Saigoh, K.; Kusunoki, S.; Ando, M.; Hiramatsu, Y.; Okamoto, Y.; Takashima, H.
Journal:
Clinical genetics
Issue:
Volume 92:Issue 6(2017)
Page Start:
659
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗