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                                       Details for article 15 of 38 found articles
 
 
  FKRP mutations cause congenital muscular dystrophy 1C and limb-girdle muscular dystrophy 2I in Asian patients
 
 
Title: FKRP mutations cause congenital muscular dystrophy 1C and limb-girdle muscular dystrophy 2I in Asian patients
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
Appeared in: Journal of clinical neuroscience
Paging: Volume 92 () nr. C pages 215-221
Year: 2021
Contents:
Publisher: Elsevier Ltd
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 15 of 38 found articles
 
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