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Autor:
Ohto, Umeharu, Usui, Kimihito, Ochi, Toshinari, Yuki, Kenjiro, Satow, Yoshinori, Shimizu, Toshiyuki
Publikováno v:
In Journal of Biological Chemistry 13 January 2012 287(3):1801-1812
Autor:
Ohto, Umeharu, Usui, Kimihito, Ochi, Toshinari, Yuki, Kenjiro, Satow, Yoshinori, Shimizu, Toshiyuki
G(M1) gangliosidosis and Morquio B are autosomal recessive lysosomal storage diseases associated with a neurodegenerative disorder or dwarfism and skeletal abnormalities, respectively. These diseases are caused by deficiencies in the lysosomal enzyme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1de2eddc4423ac82d0ca1aff9ab5a306
https://europepmc.org/articles/PMC3265862/
https://europepmc.org/articles/PMC3265862/