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Limb-girdle muscular dystrophies. Hiroyuki SORIMACHI 1,2 , Yasuko ONo 2 , Koichi SuzuKI 2 1Laboratory of Biological Function, Department of AppLied Biological Chemistry, Graduate School of Agricultural and Life Sciences, The University of Tokyo 2Laboratory of Molecular Structure and Function, Institute of Molecular and Cellular Bioscience, The University of Tokyo Keyword: カルパイン , プロテアーゼ , カルシウム結合タンパク質 , 自己消化 pp.189-203
Published Date 2000/4/10
DOI https://doi.org/10.11477/mf.1431901138
  • Abstract
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Limb-girdle muscular dystrophies (LGMD) are now classified into 13 types ; 5 autosomal dominant types (1A-1E) and 8 autosomal recessive types (2A-2H). Among them, LGMD2C-2F are called “sarcoglycanopathies”, since their responsible gene products are α-, β-, γ-, and δ-sarcoglycans, respectively, as described in the previous section.


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電子版ISSN 1882-1243 印刷版ISSN 0001-8724 医学書院

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