Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Patricia Madrazo-Clemente"'
Autor:
Alberto Ortiz, Jaime Esteban, Carmen Peláez, María del Carmen Martínez-Cuesta, Teresa Requena, John-Jairo Aguilera-Correa, Patricia Madrazo-Clemente, Maria Dolores Sanchez-Niño
Publikováno v:
Scientific Reports
Scientific Reports, Vol 10, Iss 1, Pp 1-1 (2020)
Scientific Reports, Vol 10, Iss 1, Pp 1-1 (2020)
Fabry disease is a rare X-linked lysosomal storage disorder resulting from deficient activity of α-galactosidase A, leading to the accumulation of glycosphingolipids such as globotriaosylsphingosine (lyso-Gb3). The gastrointestinal symptoms of this
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b179161bc4756cda7797f1b2763ec1a0
https://doi.org/10.1038/s41598-020-62302-6
https://doi.org/10.1038/s41598-020-62302-6
Autor:
Carmen Peláez, Jaime Esteban, Maria Dolores Sanchez-Niño, María del Carmen Martínez-Cuesta, John-Jairo Aguilera-Correa, Teresa Requena, Alberto Ortiz, Patricia Madrazo-Clemente
Publikováno v:
Scientific Reports
Scientific Reports, Vol 9, Iss 1, Pp 1-10 (2019)
Digital.CSIC. Repositorio Institucional del CSIC
instname
Scientific Reports, Vol 9, Iss 1, Pp 1-10 (2019)
Digital.CSIC. Repositorio Institucional del CSIC
instname
Parts of this work were previously presented at the 21st, 22nd, and 23rd Spanish Congress of Clinical Microbiology and Infectious Diseases, the 29th European Congress of Clinical Microbiology and Infectious Diseases, the 6th Update on Fabry Disease,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dba4f29bec9906e9a15995ccc24d3ab6
http://hdl.handle.net/10261/204921
http://hdl.handle.net/10261/204921
