Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Tsu-Min Kan"'
Autor:
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
Publikováno v:
PLoS ONE, Vol 12, Iss 8, p e0183406 (2017)
[This corrects the article DOI: 10.1371/journal.pone.0170517.].
Externí odkaz:
https://doaj.org/article/aad47b1fdccf4f6e8ada95931a624ae6
Autor:
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
Publikováno v:
PLoS ONE, Vol 12, Iss 2, p e0170517 (2017)
PURPOSE:Congenital muscular dystrophy (CMD) is a heterogeneous disease entity. The detailed clinical manifestation and causative gene for each subgroup of CMD are quite variable. This study aims to analyze the phenotypes and genotypes of Taiwanese pa
Externí odkaz:
https://doaj.org/article/b3d7bbadbb5b40678cb207ca54b72fb3
Autor:
Ichizo Nishino, Yuh-Jyh Jong, Po-Ching Chou, Yukiko K. Hayashi, Chia-Cheng Hung, Yi-Ning Su, Wen-Chen Liang, Tsu-Min Kan, Wan-Zi Chen
Publikováno v:
Journal of the Neurological Sciences. 362:304-308
Limb-girdle muscular dystrophy type 2D (LGMD2D), an autosomal-recessive inherited LGMD, is caused by the mutations in SGCA. SGCA encodes alpha-sarcoglycan (SG) that forms a heterotetramer with other SGs in the sarcolemma, and comprises part of the dy
Autor:
Xia Tian, Chung-Yee Yuo, Yuh-Jyh Jong, Lee-Jun C. Wong, Yi-Ning Su, Ichizo Nishino, Wen-Chen Liang, Tsu-Min Kan, Wan-Zi Chen
Publikováno v:
PLoS ONE
PLoS ONE, Vol 12, Iss 2, p e0170517 (2017)
PLoS ONE, Vol 12, Iss 2, p e0170517 (2017)
Purpose Congenital muscular dystrophy (CMD) is a heterogeneous disease entity. The detailed clinical manifestation and causative gene for each subgroup of CMD are quite variable. This study aims to analyze the phenotypes and genotypes of Taiwanese pa