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Autor:
Barth, Anneliese Lopes, Magalhães, Tatiana de Sá Carneiro Pacheco de, Reis, Ana Beatriz Rodrigues, Oliveira, Maria Lucia C., Scalco, Fernanda Bertao, Cavalcanti, Nicolette Celani, Silva, Daniel de Souza e, Torres, Danielle de Araujo, Costa, Alessandra Augusta Barroso Penna e, Bonfim, Carmem Maria Sales, Giugliani, Roberto, Llerena Junior, Juan Clinton, Horovitz, Dafne Dain Gandelman
Publikováno v:
Repositório Institucional da UFRGS
Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
Mucopolysaccharidosis type II (MPS II - Hunter syndrome) is an X-linked lysosomal storage disorder caused by a deficiency in the enzyme iduronate-2 sulfatase (I2S), leading to the accumulation of the glycosaminoglycans, affecting multiple organs and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3056::8282b839fb434355e0fc2c8cf72e37bd