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Autor:
Zh. Sh. Bagomedova, A. S. Kotov, M. N. Borisova, M. V. Panteleeva, N. V. Zhurkova, A. A. Byome, Yu. Yu. Kotalevskaya, O. S. Mironova, I. V. Razheva
Publikováno v:
Русский журнал детской неврологии, Vol 11, Iss 1, Pp 29-35 (2016)
Ornithine transcarbamylase deficiency (type II hyperammonemia) – X-linked metabolic disorder of the urea cycle, caused by mutations of the gene encoding ornithine transcarbamylase (OTC). Changes to the nervous system caused by degenerative processe
Externí odkaz:
https://doaj.org/article/bf2152da24fd4d9c8b17eb88987c963c
