FKRP mutations cause congenital muscular dystrophy 1C and limb-girdle muscular dystrophy 2I in Asian patients-Reference-Cited by-同舟云学术

FKRP mutations cause congenital muscular dystrophy 1C and limb-girdle muscular dystrophy 2I in Asian patients

Published:2021-10 Issue: Volume:92 Page:215-221
ISSN:0967-5868
Container-title:Journal of Clinical Neuroscience
language:en
Short-container-title:Journal of Clinical Neuroscience

Author:

Awano Hiroyuki,Saito Yoshihiko,Shimizu Mamiko,Sekiguchi Kenji,Niijima Shinichi,Matsuo Masafumi,Maegaki Yoshihiro,Izumi Isho,Kikuchi Chiya,Ishibashi Masato,Okazaki Tetsuya,Komaki Hirofumi,Iijima Kazumoto,Nishino Ichizo

Funder

National Center of Neurology and Psychiatry

Japan Agency for Medical Research and Development

Publisher

Elsevier BV

Subject

Physiology (medical),Clinical Neurology,Neurology,General Medicine,Surgery

Reference47 articles.

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3. Membrane organization of the dystrophin-glycoprotein complex;Ervasti;Cell,1991

4. Dystrophin-Glycoprotein Complex: Post-translational Processing and Dystroglycan Function;Michele;J Biol Chem,2003

5. The genetic and molecular basis of muscular dystrophy: roles of cell–matrix linkage in the pathogenesis;Kanagawa;J. Hum. Genet.,2006

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