Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Ibtissem Jaballi"'
Autor:
Latifa Chkioua, Hela Boudabous, Ibtissem Jaballi, Oussama Grissa, Hadhami Ben Turkia, Neji Tebib, Sandrine Laradi
Publikováno v:
Diagnostic Pathology, Vol 13, Iss 1, Pp 1-8 (2018)
Abstract Background The mucopolysaccharidosis type I (MPS I) is a lysosomal storage disease resulting from the defective activity of the enzyme α-L-iduronidase (IDUA). The disease has three major clinical subtypes (severe Hurler syndrome, intermedia
Externí odkaz:
https://doaj.org/article/19f742a2ac334e2fb43125117847891f
Autor:
Sandrine Laradi, Neji Tebib, Latifa Chkioua, Ibtissem Jaballi, Hadhami Ben Turkia, Hela Boudabous, Oussama Grissa
Publikováno v:
Diagnostic Pathology, Vol 13, Iss 1, Pp 1-8 (2018)
Diagnostic Pathology
Diagnostic Pathology
Background The mucopolysaccharidosis type I (MPS I) is a lysosomal storage disease resulting from the defective activity of the enzyme α-L-iduronidase (IDUA). The disease has three major clinical subtypes (severe Hurler syndrome, intermediate Hurler
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35f5c49b839884de0298bcf9d17905e2
https://doi.org/10.1186/s13000-018-0710-3
https://doi.org/10.1186/s13000-018-0710-3