Molecular genetic analysis of dysferlin in Japanese patients with Miyoshi myopathy-Reference-Cited by-同舟云学术

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Molecular genetic analysis of dysferlin in Japanese patients with Miyoshi myopathy

Published:1999 Issue:7 Volume:75 Page:207-212
ISSN:0386-2208
Container-title:Proceedings of the Japan Academy, Series B
language:en
Short-container-title:Proceedings of the Japan Academy. Ser. B: Physical and Biological Sciences

Author:

MATSUMURA Tsuyoshi¹,AOKI Masashi²,NAGANO Atsushi¹³,HAYASHI Yukiko K.¹,ASADA Chie⁴,OGAWA Megumu¹,YAMANAKA Gaku¹,GOTO Kanako¹,NAKAGAWA Masanori⁵,OKA Hisayoshi⁶,SAHASHI Ko⁷,KOUHARA Nobuo⁸,SAITO Yuko⁹,BROWN Robert H.⁴,NONAKA Ikuya¹⁰,ARAHATA Kiichi¹

Affiliation:

1. Department of Neuromuscular Research, National Institute of Neuroscience

2. Department of Neurology, Tohoku University

3. The IIIrd Department of Internal Medicine, Tokyo Medical University

4. Day Neuromuscular Research Laboratory, Massachusetts General Hospital-East

5. The IIIrd Department of Internal Medicine, Kagoshima University

6. The IIIrd Department of Internal Medicine, The Jikei University School of Medicine

7. The IVth Department of Internal Medicine, Aichi Medical University

8. Department of Neurology, Kyoto University

9. Department of Neurology, University of Tokyo

10. Department of Ultrastructural Research, National Institute of Neuroscience

Publisher

Japan Academy

Subject

General Physics and Astronomy,General Agricultural and Biological Sciences,General Medicine

Link

http://www.jstage.jst.go.jp/article/pjab1977/75/7/75_7_207/_pdf

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1. The Dysferlinopathies Conundrum: Clinical Spectra, Disease Mechanism and Genetic Approaches for Treatments;Biomolecules;2024-02-21

2. Portrait of Dysferlinopathy: Diagnosis and Development of Therapy;Journal of Clinical Medicine;2023-09-16

3. Usefulness of comprehensive targeted multigene panel sequencing for neuromuscular disorders in Korean patients;Molecular Genetics & Genomic Medicine;2019-09

4. Clinical features and a mutation with late onset of limb girdle muscular dystrophy 2B;Journal of Neurology, Neurosurgery & Psychiatry;2012-12-15

5. FER-1 regulates Ca2+-mediated membrane fusion during C. elegans spermatogenesis;Journal of Cell Science;2006-06-15

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