Mucopolysaccharidoses (MPS) are rare genetic diseases caused by the deficiency of one of the lysosomal enzymes involved in the glycosaminoglycan (GAG) breakdown pathway. This metabolic block leads to the accumulation of GAG in various organs and tissues of the affected patients, resulting in a multi...
| Main Authors: |
Giugliani, Roberto, Federhen, Andressa, Muñoz Rojas, Maria Verônica, Vieira, Taiane, Artigalás, Osvaldo, Lapagesse Pinto, Louise, Azevedo, Ana Cecília, Acosta, Angelina, Bonfim, Carmen, Lourenço, Charles Marques, Chong Ae, Kim, Horovitz, Dafne, Bonfim, Denize, Norato, Denise, Marinho, Diane, Palhares, Durval, Santos, Emerson Santana, Ribeiro, Erlane, Valadares, Eugênia, Guarany, Fábio, Lucca, Gisele Rosone de, Pimentel, Helena, Souza, Isabel Neves de, Correa Neto, Jordão, Fraga, José Carlos, Goes, José Eduardo, Cabral, José Maria, Simionato, José, Llerena Jr., Juan, Jardim, Laura, Giuliani, Liane, Silva, Luiz Carlos Santana da, Santos, Mara L., Moreira, Maria Angela, Kerstenetzky, Marcelo, Ribeiro, Márcia, Ruas, Nicole, Barrios, Patricia, Aranda, Paulo, Honjo, Rachel, Boy, Raquel, Costa, Ronaldo, Souza, Carolina, Alcantara, Flavio F., Avilla, Silvio Gilberto A., Fagondes, Simone, Martins, Ana Maria |
| Format: |
Artigo
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| Language: |
English
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| Published: |
Sociedade Brasileira de Genética
2017
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| Subjects: |
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| Online Access: |
http://repositorio.unb.br/handle/10482/27851
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