Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Paula Andrea Lerma-Barbosa"'
Autor:
María Alejandra Puentes-Tellez, Paula Andrea Lerma-Barbosa, Rafael Guillermo Garzón-Jaramillo, Diego A. Suarez, Angela J. Espejo-Mojica, Johana M. Guevara, Olga Yaneth Echeverri, Daniela Solano-Galarza, Alfredo Uribe-Ardila, Carlos J. Alméciga-Díaz
Publikováno v:
Heliyon, Vol 6, Iss 3, Pp e03635- (2020)
Lysosomal storage diseases (LSDs) are a group of about 50 inborn errors of metabolism characterized by the lysosomal accumulation of partially or non-degraded molecules due to mutations in proteins involved in the degradation of macromolecules, trans
Externí odkaz:
https://doaj.org/article/dc87a9a89f9d4088ab59aedf9db5ece1
Autor:
Olga Yaneth Echeverri, María Alejandra Puentes-Tellez, Alfredo Uribe-Ardila, Carlos J. Alméciga-Díaz, Diego Suárez, Angela J. Espejo-Mojica, Daniela Solano-Galarza, Johana Guevara, Rafael Guillermo Garzón-Jaramillo, Paula Andrea Lerma-Barbosa
Publikováno v:
Heliyon, Vol 6, Iss 3, Pp e03635-(2020)
Heliyon
Heliyon
Lysosomal storage diseases (LSDs) are a group of about 50 inborn errors of metabolism characterized by the lysosomal accumulation of partially or non-degraded molecules due to mutations in proteins involved in the degradation of macromolecules, trans
Autor:
Daniela Solano-Galarzaa, María Alejandra Puentes-Tellez, Carlos J. Alméciga-Díaz, Diego Suárez, Angela J. Espejo-Mojica, Rafael Guillermo Garzón-Jaramillo, Johana Guevara, Alfredo Uribe-Ardila, Olga Yaneth Echeverri, Paula Andrea Lerma-Barbosa
Publikováno v:
Molecular Genetics and Metabolism. 132:S88