Limb-girdle Muscular Dystrophy Type 2A with Mutation in CAPN3: The First Report in Taiwan by Chien-Hua Wang, Wen-Chen Liang, Narihiro Minami, Ichizo Nishino, Yuh-Jyh Jong

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Pediatric immune-mediated necrotizing myopathy with anti-SRP antibodies targeting 19, 68, and 72 kda subunits by Daigo Kato, Yoshitake Sato, Kanako Mitsunaga, Hiromi Aoyama, Naoko Okiyama, Ichizo Nishino, Minako Tomiita, Yuzaburo Inoue

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Retrotrans-genomics identifies aberrant THE1B endogenous retrovirus fusion transcripts in the pathogenesis of sarcoidosis by Shunsuke Funaguma, Aritoshi Iida, Yoshihiko Saito, Jantima Tanboon, Francia Victoria De Los Reyes, Kyuto Sonehara, Yu-ichi Goto, Yukinori Okada, Shinichiro Hayashi, Ichizo Nishino

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Correction: Comprehensive target capture/next-generation sequencing as a second-tier diagnostic approach for congenital muscular dystrophy in Taiwan. by Wen-Chen Liang, Xia Tian, Chung-Yee Yuo, Wan-Zi Chen, Tsu-Min Kan, Yi-Ning Su, Ichizo Nishino, Lee-Jun C Wong, Yuh-Jyh Jong

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Profiling of pathogenic variants in Japanese patients with sarcoglycanopathy by Rui Shimazaki, Yoshihiko Saito, Tomonari Awaya, Narihiro Minami, Ryo Kurosawa, Motoyasu Hosokawa, Hiroaki Ohara, Shinichiro Hayashi, Akihide Takeuchi, Masatoshi Hagiwara, Yukiko K. Hayashi, Satoru Noguchi, Ichizo Nishino

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Defects of Vps15 in skeletal muscles lead to autophagic vacuolar myopathy and lysosomal disease by Ivan Nemazanyy, Bert Blaauw, Cecilia Paolini, Catherine Caillaud, Feliciano Protasi, Amelie Mueller, Tassula Proikas‐Cezanne, Ryan C. Russell, Kun‐Liang Guan, Ichizo Nishino, Marco Sandri, Mario Pende, Ganna Panasyuk

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