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pro vyhledávání: '"Konstantin V. Jerdev"'
Autor:
Nato D. Vashakmadze, Leyla S. Namazova-Baranova, Anait K. Gevorkian, Ludmila M. Kuzenkova, Tatiana V. Podkletnova, Marina A. Babaykina, Anatoly B. Anikin, Galina B. Kuznetsova, Liliya A. Osipova, Konstantin V. Jerdev
Publikováno v:
Вопросы современной педиатрии, Vol 15, Iss 6, Pp 562-567 (2016)
Mucopolysaccharidosis type I is inherited in an autosomal recessive manner and results from the defective activity of the enzyme alpha-L-iduronidase, which leads to the accumulation of glycosaminoglycans (mainly heparan and dermatan sulfate) in the l
Externí odkaz:
https://doaj.org/article/125e57dd308e424d903a25f23de8b293
