Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Ihor Yevstihnieiev"'
Autor:
Oleksii Khaniukov, Valerii Chornyi, Ihor Yevstihnieiev, Ihor Hutnik, Oleksandra Smolianova, Nataliia Romuz, Kateryna Esterkina, Kateryna Pervieieva
Publikováno v:
Journal of V. N. Karazin Kharkiv National University: Series Medicine, Vol 41, Pp 115-122 (2021)
Background. Lesch-Nyhan syndrome is inherent X-linked recessive genetic disorder with decreased activity of hypoxanthine-guanine phosphoribosyltransferase (HGPRT). The disease is characterized by presence of the classical triad: hyperuricemia, neurol
Externí odkaz:
https://doaj.org/article/e1ff0e65a17c4914bd65645e208c3d6a
Autor:
Ihor Hutnik, Oleksandra Smolianova, Kateryna Esterkina, Kateryna Pervieieva, Oleksii Khaniukov, Valerii Chornyi, Ihor Yevstihnieiev, Nataliia Romuz
Publikováno v:
Journal of V. N. Karazin Kharkiv National University: Series Medicine, Vol 41, Pp 115-122 (2021)
Background. Lesch-Nyhan syndrome is inherent X-linked recessive genetic disorder with decreased activity of hypoxanthine-guanine phosphoribosyltransferase (HGPRT). The disease is characterized by presence of the classical triad: hyperuricemia, neurol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2370e7c15b1917a3d8419a26b101020
https://periodicals.karazin.ua/medicine/article/view/16891
https://periodicals.karazin.ua/medicine/article/view/16891