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pro vyhledávání: '"Bojović, Lana P."'
Publikováno v:
Kragujevac Journal of Science, Vol 2023, Iss 45, Pp 327-333 (2023)
Mucopolysaccharidosis type II or Hunter syndrome is a hereditary, progressive disease that occurs due to the deposition of acidic glucosaminoglycans in lysosomes, due to hereditary deficits of specific degradation enzymes. A two-year-old boy was hosp
Externí odkaz:
https://doaj.org/article/ec6a24e41f1141e2875470ffa75f286f
MUCOPOLYSACCHARIDOSIS TYPE II (HUNTER SYNDROME) IN A BOY FROM THE REPUBLIC OF SERBIA: A CASE REPORT.
Autor:
Vukajlović, Jovana M. Tubić1 jovana.tubic@pmf.kg.ac.rs, Bojović, Lana P.2, Jevremović, Nevena G.2, Simić, Ivan B.3,4
Publikováno v:
Kragujevac Journal of Science. 2023, Vol. 45, p327-333. 7p.