Genetic spectrum of Charcot–Marie–Tooth disease associated with myelin protein zero gene variants in Japan-Reference-Cited by-同舟云学术

Genetic spectrum of Charcot–Marie–Tooth disease associated with myelin protein zero gene variants in Japan

Published:2020-11-27 Issue:3 Volume:99 Page:359-375
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clinical Genetics

Author:

Taniguchi Takaki¹^ORCID,Ando Masahiro¹^ORCID,Okamoto Yuji¹²,Yoshimura Akiko¹^ORCID,Higuchi Yujiro¹,Hashiguchi Akihiro¹,Shiga Kensuke³⁴,Hayashida Arisa⁵,Hatano Taku⁵,Ishiura Hiroyuki⁶,Mitsui Jun⁶,Hattori Nobutaka⁵,Mizuno Toshiki⁴,Nakagawa Masanori⁴⁷,Tsuji Shoji⁶⁸,Takashima Hiroshi¹

Affiliation:

1. Department of Neurology and Geriatrics Kagoshima University Graduate School of Medical and Dental Sciences Kagoshima Japan

2. Department of Physical Therapy, School of Health Sciences, Faculty of Medicine Kagoshima University Kagoshima Japan

3. Department of Neurology Matsushita Memorial Hospital Osaka Japan

4. Department of Neurology Kyoto prefectural University of Medicine Kyoto Japan

5. Department of Neurology Juntendo University School of Medicine Tokyo Japan

6. Department of Molecular Neurology, Graduate School of Medicine The University of Tokyo Tokyo Japan

7. North Medical Center Kyoto prefectural University of Medicine Kyoto Japan

8. Institute of Medical Genomics International University of Health and Welfare Chiba Japan

Funder

Japan Society for the Promotion of Science

Publisher